The following data is part of a premarket notification filed by Hausmann Industries, Inc. with the FDA for Powermatic Examination Table.
Device ID | K933727 |
510k Number | K933727 |
Device Name: | POWERMATIC EXAMINATION TABLE |
Classification | Table, Powered |
Applicant | HAUSMANN INDUSTRIES, INC. 55 NORTHERN BLVD. SUITE 410 Great Neck, NY 11021 |
Contact | Alan P Schwartz |
Correspondent | Alan P Schwartz HAUSMANN INDUSTRIES, INC. 55 NORTHERN BLVD. SUITE 410 Great Neck, NY 11021 |
Product Code | INQ |
CFR Regulation Number | 890.3760 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1993-08-02 |
Decision Date | 1994-02-09 |