Atlas FDA

PHOSPHATASE PROCEDURE, TEKPOINT ALKALINE

FDA 510(k) clearance K770453 · decided 1977-05-03

Clearance details

K-number
K770453
Device name
PHOSPHATASE PROCEDURE, TEKPOINT ALKALINE
Applicant
Icn Pharmaceuticals, Inc.
Decision
Substantially Equivalent
Date received
1977-03-08
Decision date
1977-05-03
Days to decision
56 days
Clearance type
Traditional
Product code
CIO
Device class
2
Regulation number
862.1050
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Orangeburg, NY, 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
ALKALINE PHOSPHATASE, THYMOLPHTHALEIN MONOPHOSPHAT (K880177)Tech-Co, Inc.1988-04-05
ALKALINE PHOSPHATASE REAGENT SET (K860351)Sterling Diagnostics, Inc.1986-02-11
ALKALINE PHOSPHATASE REAGENT SET (K855192)Technostics Intl.1986-01-14
SANDARE ALKALINE PHOSPHATASE PROCEDURE (K844498)Sandare Chemical Co., Inc.1984-12-10
ALKALINE PHOSPHATASE REAGENT SET (K844237)Livonia Diagnostics, Inc.1984-11-20
ALKALINE PHOSPHOTASE REAGENT SET (K841064)Medical Specialties, Inc.1984-05-01
COBAS STANDARDS FOR CALCIUM-IN-ORGANIC (K823578)Hoffmann-La Roche, Inc.1983-01-07
ALKALINE PHOSPHOTASE REAGENT SET (K821200)Omega Medical Electronics1982-07-13
ALP TEST (K781324)Analytical & Research Chemicals, Inc.1978-08-31
ALKALINE PHOSPHATASE TEST SET (K772257)Stanbio Laboratory1977-12-22

Recalls involving this device

No recalls on record reference this clearance.