FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

EARLY DETECTOR

K Number: K833369 · Decision Aug 2, 1984
Classifications
1
FEI Numbers
62
Registration Numbers
62
Same Product Code
96
Applicant Total
50
Review Days
310

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
EARLY DETECTOR
K Number
K833369
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
864.6550
Medical Specialty
Hematology
Decision
Substantially Equivalent
Applicant
Warner-Lambert Co.
Date Received
September 27, 1983
Decision Date
August 2, 1984
Product Code
KHE
Advisory Committee
Hematology
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KHE Reagent, Occult Blood

Similar 510(k) Clearances

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

View all

Other Clearances by Warner-Lambert Co.

K Number Device Name
K024160 NEOSPORIN SCAR SOLUTION
K893452 EXTRA STRENGTH EFFERGRIP DENTURE ADHESIVE CREAM
K870584 O.P.T.(TM) OVULATION PREDICTION TEST
K861510 MULTILUMEN VIAPIC CENTRAL LINE CATHETER
K852689 GENERAL DIAGNOSTICS CEFTAZIDIME 30 MCG SUSC DISK
K852967 GENERAL DIAGNOSTICS' CEFTRIAXONE 30MCG SUSDEP DISK
K852843 GENERAL DIAGNOSTICS COAG-A-MATE XC
K852889 GENERAL DIAGNOSTICS RAPID E. COLI TEST
K850409 GEN. DIAG. CHROMOSTRATE REF. PLASMA
K850412 GEN. DIAG. CHROMOSTRATE ANTITHROMBIN III ASSAY
Search all 50 clearances from Warner-Lambert Co. →