FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

IRON CALIBRATOR & CALIBRATION VERIFICATION SET

K Number: K955796 · Decision Feb 29, 1996
Classifications
1
FEI Numbers
269
Registration Numbers
269
Same Product Code
492
Applicant Total
111
Review Days
69

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Basic Information

Device Name
IRON CALIBRATOR & CALIBRATION VERIFICATION SET
K Number
K955796
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
862.1660
Medical Specialty
Clinical Chemistry
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Data Medical Associates, Inc.
Date Received
December 22, 1995
Decision Date
February 29, 1996
Product Code
JJX
Advisory Committee
Clinical Chemistry
Review Advisory Committee
CH
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
JJX Single (Specified) Analyte Controls (Assayed And Unassayed)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (JJX), ordered by most recent decision date.

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Other Clearances by Data Medical Associates, Inc.

K Number Device Name
K993098 HDL-C/LDL-C CALIBRATOR, MODEL 1913-003
K971113 DMA TRIGLYCERIDES PROCEDURES
K961919 DMA GAMMA GLUTAMYLTRANSFERASE (GGT) PROCEDURE
K955302 SERUM BICARBONATE/CARBON DIOXIDE
K955300 TOTAL BILIRUBIN PROCEDURE
K952437 DMA GLUCOSE HEXOKINASE U.V. PROCEDURE
K946161 DMA TOTAL CHOLESTEROL PROCEDURE
K946354 DMA UNSATURATED IRON BINDING CAPACITY PROCEDURE
K946355 DMA ALBUMIN PROCEDURE
K944255 DMA CALCIUM PLUS PROCEDURE
Search all 111 clearances from Data Medical Associates, Inc. →