Atlas FDA

IMMULITE C-PEPTIDE

FDA 510(k) clearance K943767 · decided 1995-03-23

Clearance details

K-number
K943767
Device name
IMMULITE C-PEPTIDE
Applicant
Diagnostic Products Corp.
Decision
Substantially Equivalent
Date received
1994-08-02
Decision date
1995-03-23
Days to decision
233 days
Clearance type
Traditional
Product code
JKD
Device class
1
Regulation number
862.1135
Medical specialty
Clinical Chemistry
Advisory committee
Clinical Chemistry
Location
Los Angeles, CA, 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
AIA-PACK CPR ASSAY (K951848)Tosoh Medics, Inc.1996-02-13
DSL C-PEPTIDE RIA (DSL #7000) (K896420)Diagnostic Systems Laboratories, Inc.1990-05-24
DOUBLE ANTIBODY C-PEPTIDE RIA KIT (K854066)Diagnostic Products Corp.1985-11-12
C-PEP-RIA-100 (K842267)Institut National Des Radioelements1984-09-06
C-PEPTIDE RADIOIMMUNOASSAY TEST KIT (K833396)Serono Diagnostics, Inc.1984-04-13
HUMAN C-PEPTIDE OF INSULIN BY RADIOIMM. (K820666)Immuno Nuclear Corp.1982-07-13
RIA QUANT C-PEPTIDE KIT (K812689)Mallinckrodt Critical Care1981-10-06
HUMAN C-PEPTIDE REAGENTS (K812288)Immunex Radiochemical Diagnostics1981-08-31
C-PEPTICE REAGENTS (K810718)Calbiochem-Behring Corp.1981-03-31

Recalls involving this device

No recalls on record reference this clearance.