PIPETTER-DILUTER (MODEL 273)
FDA 510(k) clearance K761019 · decided 1976-11-16
Clearance details
- K-number
- K761019
- Device name
- PIPETTER-DILUTER (MODEL 273)
- Applicant
- Beckman Instruments, Inc.
- Decision
- Substantially Equivalent
- Date received
- 1976-11-11
- Decision date
- 1976-11-16
- Days to decision
- 5 days
- Clearance type
- Traditional
- Product code
- JRW
- Device class
- 1
- Regulation number
- 866.3065
- Medical specialty
- Microbiology
- Advisory committee
- Microbiology
- Location
- Mchenry, IL, 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 |
|---|---|---|
| CULTURE SWAB (K780713) | Royal Scientific, Inc. | 1978-05-12 |
Recalls involving this device
No recalls on record reference this clearance.