ALPHA AMYLASE
FDA 510(k) clearance K863052 · decided 1986-09-09
Clearance details
- K-number
- K863052
- Device name
- ALPHA AMYLASE
- Applicant
- J. D. Assoc.
- Decision
- Substantially Equivalent
- Date received
- 1986-08-12
- Decision date
- 1986-09-09
- Days to decision
- 28 days
- Clearance type
- Traditional
- Product code
- CJA
- Device class
- 2
- Regulation number
- 862.1070
- Medical specialty
- Clinical Chemistry
- Advisory committee
- Clinical Chemistry
- Location
- Montclair, NJ, 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 |
|---|---|---|
| MODIFIED HI CHEM AMYLASE REAGENT (PRODUCT #88129) (K895555) | Hichem Diagnostics | 1989-12-22 |
| AMYLASE REAGENT KIT FOR ASTRA SYSTEMS (K884226) | A-Kem, Inc. | 1988-12-09 |
| WAKO(TM) AUTOKIT AMYLASE (K883059) | Wako Chemicals USA, Inc. | 1988-08-30 |
| PARAMAX AMYLASE REAGENT (K873520) | Baxter Healthcare Corp | 1987-11-23 |
| AMYLASE LTS (K862640) | Electro-Nucleonics Laboratories, Inc. | 1986-09-09 |
| AMYLASE REAGENT SET (MODIFIED CARAWAY) (K860530) | Sterling Diagnostics, Inc. | 1986-02-28 |
| AMYLASE REAGENT CS-726 (K844168) | Fisher Scientific Co., LLC | 1984-11-20 |
| ASTRA SYSTEMS AMYLASE REAGENT KIT (K843529) | Beckman Instruments, Inc. | 1984-10-11 |
| AMYLASE REAGENT SET-MODIFIED CARAWAY (K833864) | Sterling Biochemical, Inc. | 1984-01-13 |
Recalls involving this device
No recalls on record reference this clearance.