MYCOPLASMA PNEUMONIAE
FDA 510(k) clearance K843664 · decided 1984-10-25
Clearance details
- K-number
- K843664
- Device name
- MYCOPLASMA PNEUMONIAE
- Applicant
- Institute Virion , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1984-09-17
- Decision date
- 1984-10-25
- Days to decision
- 38 days
- Clearance type
- Traditional
- Product code
- GSB
- Device class
- 1
- Regulation number
- 866.3375
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
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Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| MYCOPLASMA SPP SEROLOGICAL REAGENTS (K852933) | Microbix Biosystems, Inc. | 1985-08-01 |
| MYCOPLASMA PNEUMONIAE CF ANTIGEN (K834338) | Hillcrest Biologicals | 1984-02-27 |
| SERA-TEK MYCOPLASMA ANTIBODY TEST (K832132) | Miles Laboratories, Inc. | 1983-09-20 |
| MYCOPLASMA PNEUMONIAE ANTIGEN & CONTROL (K802934) | Orion Diagnostica, Inc. | 1980-12-31 |
Recalls involving this device
No recalls on record reference this clearance.