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

TINSDALE ENRICHMENT

K Number: K834066 · Decision Jan 4, 1984
Classifications
1
FEI Numbers
15
Registration Numbers
15
Same Product Code
69
Applicant Total
137
Review Days
40

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
TINSDALE ENRICHMENT
K Number
K834066
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2450
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
Remel Co.
Date Received
November 25, 1983
Decision Date
January 4, 1984
Product Code
JSK
Advisory Committee
Microbiology
Review Advisory Committee
MI
Third Party
N

Classifications

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

Product Code Device Name
JSK Supplement, Culture Media

Similar 510(k) Clearances

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

View all

Other Clearances by Remel Co.

K Number Device Name
K013711 BACTI-SWAB DRY
K965150 A.C.T. IV
K965151 A.C.T. III
K965152 A.C.T. II
K965149 A.C.T. I
K960090 CALCOFLUOR WHITE STAIN KIT
K960095 BACTIDROP CALCOFLUOR WHITE
K955669 REMEL CEFEPIME 30 UG SUSCEPTIBILITY DISK
K941443 SYNERGY QUAD
K941444 BHI AGAR WITH VANCOMYCIN
Search all 137 clearances from Remel Co. →