The following data is part of a premarket notification filed by Nunc, Inc. with the FDA for Tissue Culture Tubes.
| Device ID | K873889 |
| 510k Number | K873889 |
| Device Name: | TISSUE CULTURE TUBES |
| Classification | Flask, Tissue Culture |
| Applicant | NUNC, INC. ATTORNEY AT LAW 2085 RUSTIN AVENUE Riverside, CA 92507 |
| Contact | Stanley E Fry |
| Correspondent | Stanley E Fry NUNC, INC. ATTORNEY AT LAW 2085 RUSTIN AVENUE Riverside, CA 92507 |
| Product Code | KJA |
| CFR Regulation Number | 864.2240 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1987-09-23 |
| Decision Date | 1987-11-25 |