GASTRIN EIA MODEL 06B-555017
FDA 510(k) clearance K961276 · decided 1996-05-30
Clearance details
- K-number
- K961276
- Device name
- GASTRIN EIA MODEL 06B-555017
- Applicant
- Biosyn , Ltd.
- Decision
- Substantially Equivalent
- Date received
- 1996-04-03
- Decision date
- 1996-05-30
- Days to decision
- 57 days
- Clearance type
- Traditional
- Product code
- CGC
- Device class
- 1
- Regulation number
- 862.1325
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Belfast, IE
- Third-party review
- No
- Expedited review
- No
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|---|---|---|
| GASTRIN 34 HORMONE BY RADIOUMMUNOASSAY (K842079) | Immuno Nuclear Corp. | 1984-06-26 |
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| DPC GASTRIN KIT (K833489) | Diagnostic Products Corp. | 1984-01-30 |
| BLOOD GAS & FLAME PHOTOMETER INSTRU- (K831075) | United Diagnostics, Inc. | 1983-06-22 |
| GASTRIN RADIOIMMUNOASSAY KIT (125-I) (K821175) | Bd Becton Dickinson Vacutainer Systems Preanalytic | 1982-05-14 |
| GASTRIN 1-17 BY RADIOIMMUNOASSAY KIT (K812727) | Immuno Nuclear Corp. | 1981-11-05 |
| GASTRIN RIA DIAGNOSTIC KIT (K812004) | Abbott Laboratories | 1981-07-28 |
| GASTRIN RADIOIMMUNOASSAY TEST (K810722) | Clinical Assays, Inc. | 1981-05-27 |
| GASTRIN RIA MODULE (K771953) | Inter Science Institute | 1978-01-20 |
Recalls involving this device
No recalls on record reference this clearance.