The following data is part of a premarket notification filed by Micromedics, Inc. with the FDA for Surgical Sealant Applicator.
Device ID | K883338 |
510k Number | K883338 |
Device Name: | SURGICAL SEALANT APPLICATOR |
Classification | Syringe, Irrigating (non Dental) |
Applicant | MICROMEDICS, INC. 268 E. LAFAYETTE FRONTAGE ROAD St. Paul, MN 55107 |
Contact | Curtis H Miller |
Correspondent | Curtis H Miller MICROMEDICS, INC. 268 E. LAFAYETTE FRONTAGE ROAD St. Paul, MN 55107 |
Product Code | KYZ |
CFR Regulation Number | 880.6960 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1988-08-09 |
Decision Date | 1988-08-23 |