During the last decade, single-photon double ionization (DPI) of atoms and molecules has attracted much attention from both experimentalists and theorists. This was stimulated by the advent of VUV radiation sources that produce photons having well-defined polarization as well as by the development of techniques for coincidence measurements. Kinematically complete experiments allow one to gain much insight into the physical mechanisms of DPI by studying the photoelectron angular distributions described by the triply differential cross section (TDCS) [1][2][3]. Until recently, however, all experimental studies of the TDCS for DPI have been interpreted within the electric-dipole approximation (EDA) (see, e.g., recent experimental measurements [4-6] of the TDCS for DPI of He at excess energies of 100 eV and 450 eV with which convergent close-coupling (CCC) EDA predictions have been compared). Only recently have theoretical analyses of lowest order nondipole effects in the TDCS been reported [7][8][9]. The analytic analyses presented in these works have established the general angular-polarization structure of both the dipole-quadrupole transition amplitude and the TDCS for DPI from the 1 S 0 two-electron bound state. The corresponding numerical analyses [7][8][9] have so far employed only a perturbative (in the interelectron interaction) dynamical model of the DPI process, whose gauge-invariant predictions for photon energies of the order of hundreds of eV are reliable only for large mutual ejection angles [8]. Thus, while predicting quite significant nondipole asymmetries in photoelectron angular distributions, the perturbative 0953-4075/06/020035+09$30.00