The following data is part of a premarket notification filed by Pneu Pac, Ltd. with the FDA for Compressor.
Device ID | K792457 |
510k Number | K792457 |
Device Name: | COMPRESSOR |
Classification | Compressor, Air, Portable |
Applicant | PNEU PAC, LTD. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
Product Code | BTI |
CFR Regulation Number | 868.6250 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1979-12-03 |
Decision Date | 1980-02-05 |