The following data is part of a premarket notification filed by Instrument Makar, Inc. with the FDA for Gravity Assist.
Device ID | K902854 |
510k Number | K902854 |
Device Name: | GRAVITY ASSIST |
Classification | Syringe, Irrigating (non Dental) |
Applicant | INSTRUMENT MAKAR, INC. 2950 EAST MT. HOPE RD. Okemos, MI 48864 |
Contact | Dean Look |
Correspondent | Dean Look INSTRUMENT MAKAR, INC. 2950 EAST MT. HOPE RD. Okemos, MI 48864 |
Product Code | KYZ |
CFR Regulation Number | 880.6960 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1990-06-29 |
Decision Date | 1990-08-29 |