The following data is part of a premarket notification filed by Rand Scientific Corp. with the FDA for Pec Implant.
Device ID | K961072 |
510k Number | K961072 |
Device Name: | PEC IMPLANT |
Classification | Implant, Muscle, Pectoralis |
Applicant | RAND SCIENTIFIC CORP. 4135 NORTHGATE BLVD. SUITE 9 Sacramento, CA 95834 |
Contact | Duane Tracy |
Correspondent | Duane Tracy RAND SCIENTIFIC CORP. 4135 NORTHGATE BLVD. SUITE 9 Sacramento, CA 95834 |
Product Code | MIC |
CFR Regulation Number | 874.3620 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1996-03-18 |
Decision Date | 1996-04-19 |