PANTRAK E.K.
FDA 510(k) clearance K810669 · decided 1981-03-31
Clearance details
- K-number
- K810669
- Device name
- PANTRAK E.K.
- Applicant
- Calbiochem-Behring Corp.
- Decision
- Substantially Equivalent
- Date received
- 1981-03-12
- Decision date
- 1981-03-31
- Days to decision
- 19 days
- Clearance type
- Traditional
- Product code
- CIW
- Device class
- 2
- Regulation number
- 862.1070
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Walker, MI, US
- Third-party review
- No
- Expedited review
- No
+ Add to Predicate Builder ◉ Watch Calbiochem-Behring Corp.
Need this as data, not a web page?
Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.
Similar devices under this product code
Devices cleared under the same product code - the starting set for predicate research.
| Record | Firm | Date |
|---|---|---|
| DMA AMYLASE PROCEDURE (K931559) | Data Medical Associates, Inc. | 1993-10-28 |
| OLYMPUS AMYLASE REAGENT (K924339) | Olympus Corp. | 1992-10-19 |
| AMYLASE TEST (AMYL) ITEM NUMBER: 65653 (K884382) | Em Diagnostic Systems, Inc. | 1989-01-11 |
| ENZYMATIC ALPHA-AMYLASE REAGENT KIT (K850639) | Bio-Analytics Laboratories, Inc. | 1985-03-05 |
| KODAK EKTACHEM CLIN. CHEM. SLIDES (AMYL) (K812027) | Eastman Kodak Company | 1981-08-03 |
| PHADEBAS ISOAMYLASE TEST (K810584) | Pharmacia, Inc. | 1981-05-13 |
| UNITEST AMYLASE (K782032) | Boehringer Mannheim Corp. | 1979-03-02 |
Recalls involving this device
No recalls on record reference this clearance.