The following data is part of a premarket notification filed by Hardy Diagnostics with the FDA for Thayer Martin, Modified Pill Pocket.
| Device ID | K934331 |
| 510k Number | K934331 |
| Device Name: | THAYER MARTIN, MODIFIED PILL POCKET |
| Classification | Culture Media, For Isolation Of Pathogenic Neisseria |
| Applicant | HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
| Contact | Melissa M Traylor |
| Correspondent | Melissa M Traylor HARDY DIAGNOSTICS 1430 WEST MCCOY LN. Santa Maria, CA 93455 |
| Product Code | JTY |
| CFR Regulation Number | 866.2410 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1993-09-03 |
| Decision Date | 1993-12-21 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816576020058 | K934331 | 000 |
| 00816576020072 | K934331 | 000 |