Snap Mycobacteria Avium Complex
FDA 510(k) K900202 · Syngene, Inc.
510(k) numberK900202
Submission
- Device name
- Snap Mycobacteria Avium Complex
- Applicant
- Syngene, Inc.
San Diego, CA, US - Received
- January 16, 1990
- Decision date
- April 3, 1990
- Decision
- Substantially Equivalent (SESE)
- Type
- Traditional 510(k)
Device classification
- Product code
- LQF – Dna-Reagents, Mycobacterium Spp.
- Device class
- Class I (low risk)
- Regulation
- 21 CFR 866.3370
- Specialty
- Microbiology
Other 510(k)s with product code LQF
| 510(k) | Device | Applicant | Decision |
|---|---|---|---|
| K921435 | Accuprobe Mycobacterium Avium Complex CultureLQF · Traditional | Gen-Probe, Inc. | 07/23/1992SE |
| K904463 | Accuprobe Mycobacterium Kansasii Cult Confirm TestLQF · Traditional | Gen-Probe, Inc. | 11/13/1990SE |
| K897077 | Accuprobe Mycobacterium Intracellulare CultureLQF · Traditional | Gen-Probe, Inc. | 08/23/1990SE |
| K896494 | Accuprobe Mycobacterium Avium Culture TestLQF · Traditional | Gen-Probe, Inc. | 08/23/1990SE |
| K897078 | Accuprobe Mycobacterium Avium Complex CultureLQF · Traditional | Gen-Probe, Inc. | 05/02/1990SE |
| K896492 | Accuprobe Mycobacterium Gordonae Culture TestLQF · Traditional | Gen-Probe, Inc. | 04/16/1990SE |
| K896493 | Accuprobe Mycobacterium Tuberculosis Complex TestLQF · Traditional | Gen-Probe, Inc. | 04/11/1990SE |
| K900292 | Snap M. Tuberculosis ComplexLQF · Traditional | Syngene, Inc. | 04/03/1990SE |
| K890089 | Rapid Diag. System for Mycobacterium GordonaeLQF · Traditional | Gen-Probe, Inc. | 03/13/1989SE |
| K871795 | Rapid Diagnostic System for Mycobacterium Tuber.LQF · Traditional | Gen-Probe, Inc. | 07/30/1987SE |
More from Gen-Probe, Inc.
| 510(k) | Device | Decision |
|---|---|---|
| K900292 | Snap M. Tuberculosis ComplexLQF · Traditional | 04/03/1990SE |
Questions and answers
When was Snap Mycobacteria Avium Complex cleared by the FDA?
Snap Mycobacteria Avium Complex (K900202) received a 510(k) decision of Substantially Equivalent on April 3, 1990, 77 days after the submission was received.
What is the product code of K900202?
The FDA product code is LQF – Dna-Reagents, Mycobacterium Spp., a Class I (low risk) device regulated under 21 CFR 866.3370.