The following data is part of a premarket notification filed by Ugm Medical Systems, Inc. with the FDA for Penn-pet Scanner.
Device ID | K890100 |
510k Number | K890100 |
Device Name: | PENN-PET SCANNER |
Classification | System, Tomography, Computed, Emission |
Applicant | UGM MEDICAL SYSTEMS, INC. 404 OAK LN. Wayne, PA 19087 |
Contact | Gerd Muehllehner |
Correspondent | Gerd Muehllehner UGM MEDICAL SYSTEMS, INC. 404 OAK LN. Wayne, PA 19087 |
Product Code | KPS |
CFR Regulation Number | 892.1200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-01-10 |
Decision Date | 1989-04-13 |