The following data is part of a premarket notification filed by Immuno-mycologics, Inc. with the FDA for Ya-crypto Antibody Tube Agglutination.
| Device ID | K810510 |
| 510k Number | K810510 |
| Device Name: | YA-CRYPTO ANTIBODY TUBE AGGLUTINATION |
| Classification | Antisera, Latex Agglutination, Cryptococcus Neoformans |
| Applicant | IMMUNO-MYCOLOGICS, INC. 803 N. Front St. Suite 3 Mchenry, IL 60050 |
| Product Code | GMD |
| CFR Regulation Number | 866.3165 [🔎] |
| Decision | Substantially Equivalent (SESE) |
| Type | Traditional |
| 3rd Party Reviewed | No |
| Combination Product | No |
| Date Received | 1981-02-24 |
| Decision Date | 1981-03-20 |
| Device Identifier | submissionNumber | Supplement |
|---|---|---|
| 00816387020872 | K810510 | 000 |