Atlas FDA

PHADEBAS ISOAMYLASE TEST

FDA 510(k) clearance K810584 · decided 1981-05-13

Clearance details

K-number
K810584
Device name
PHADEBAS ISOAMYLASE TEST
Applicant
Pharmacia, Inc.
Decision
Substantially Equivalent
Date received
1981-03-04
Decision date
1981-05-13
Days to decision
70 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
PANTRAK E.K. (K810669)Calbiochem-Behring Corp.1981-03-31
UNITEST AMYLASE (K782032)Boehringer Mannheim Corp.1979-03-02

Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
MODELS 011 & 011B IRIDOCAPSULAR IOLS (P810042)Pharmacia, Inc.1982-12-15