Atlas FDA

WAKO INSULIN TEST

FDA 510(k) clearance K823939 · decided 1983-01-28

Clearance details

K-number
K823939
Device name
WAKO INSULIN TEST
Applicant
Wako Chemicals USA, Inc.
Decision
Substantially Equivalent
Date received
1982-12-29
Decision date
1983-01-28
Days to decision
30 days
Clearance type
Traditional
Product code
CFP
Device class
1
Regulation number
862.1405
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
ALPCO/MERCODIA INSULIN ELISA (K963911)American Laboratory Products Co., Ltd.1996-11-01
ACCESS ULTRASENSITIVE INSULIN ASSAY (K953084)Bio-Rad Laboratories, Inc.1995-09-25
IMX INSULIN (K920109)Abbott Laboratories1992-05-07
DSL INSULIN RIA (DSL 1600) (K914820)Diagnostic Systems Laboratories, Inc.1992-01-09
AIA-PACK IRI (K903628)Tosoh Corp.1990-09-07
ENZYMUN TEST(R) INSULIN (K901135)Boehringer Mannheim Corp.1990-04-03
REP(TM) SPE PLUS-30 PROCEDURES (K896572)Helena Laboratories1990-01-11
RIA-GNOST INSULIN (K890837)Cambridge Medical Technology1989-04-26
PHARMACIA INSULIN RIA (K851071)Pharmacia, Inc.1985-04-12
INSULIN RADIOIMMUNOASSAY KIT (K841573)Sorin Biomedica, Fiat, USA, Inc.1984-05-16
COVALENT COAT RIA KIT (K822509)Immuchem Corp.1982-09-28
COAT-A-COUNT INSULIN KIT (K821861)Diagnostic Products Corp.1982-07-08

Recalls involving this device

No recalls on record reference this clearance.