Atlas FDA

UNITEST AMYLASE

FDA 510(k) clearance K782032 · decided 1979-03-02

Clearance details

K-number
K782032
Device name
UNITEST AMYLASE
Applicant
Boehringer Mannheim Corp.
Decision
Substantially Equivalent
Date received
1978-12-06
Decision date
1979-03-02
Days to decision
86 days
Clearance type
Traditional
Product code
CIW
Device class
2
Regulation number
862.1070
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
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.

RecordFirmDate
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 Company1981-08-03
PHADEBAS ISOAMYLASE TEST (K810584)Pharmacia, Inc.1981-05-13
PANTRAK E.K. (K810669)Calbiochem-Behring Corp.1981-03-31

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
ENZYMUN TEST{R} CEA (P860058/S001)Boehringer Mannheim Corp.1993-07-29
ENZYMUN-TEST{R} AFP (P860044/S003)Boehringer Mannheim Corp.1991-09-03
ENZYMUN-TEST{R} AFP (P860044/S002)Boehringer Mannheim Corp.1991-07-19
ENZYMUN-TEST{R} AFP (P860044/S001)Boehringer Mannheim Corp.1990-08-03
MICUR-MIC SYSTEMS (P820073)Boehringer Mannheim Corp.1983-06-29