The following data is part of a premarket notification filed by Mikro-tek Laboratories with the FDA for Mikro-lavage-1.
Device ID | K895755 |
510k Number | K895755 |
Device Name: | MIKRO-LAVAGE-1 |
Classification | Catheter, Irrigation |
Applicant | MIKRO-TEK LABORATORIES 220 SOUTH LORI LN. Bloomington, IN 47401 |
Contact | Thomas P Clement |
Correspondent | Thomas P Clement MIKRO-TEK LABORATORIES 220 SOUTH LORI LN. Bloomington, IN 47401 |
Product Code | GBX |
CFR Regulation Number | 878.4200 [🔎] |
Decision | Substantially Equivalent (SESE) |
Type | Traditional |
3rd Party Reviewed | No |
Combination Product | No |
Date Received | 1989-09-26 |
Decision Date | 1989-12-27 |