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

VISI-SPOT

K Number: K932752 · Decision Nov 5, 1993
Classifications
1
FEI Numbers
28
Registration Numbers
28
Same Product Code
243
Applicant Total
18
Review Days
170

Basic Information

Device Name
VISI-SPOT
K Number
K932752
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2660
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
J.S. MEDICAL ASSOC.
Date Received
May 19, 1993
Decision Date
November 5, 1993
Product Code
JTO
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
JTO Discs, Strips And Reagents, Microorganism Differentiation

Similar 510(k) Clearances

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

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Other Clearances by J.S. MEDICAL ASSOC.

K Number Device Name
K932688 EYE SPOT IM TEST
K932180 EYE SPOT CRP TEST
K932551 ACCUTEX IM LATEX TEST
K926112 ACCUTEX BETA-HCG TEST
K924332 ACCUTEX CRP LATEX TEST
K924247 ACCUTEX ASO LATEX TEST
K924036 ACCUTEX RHEUMATIOD FACTOR (RF) LATEX TEST
K924037 ACCUTEX IM RBC TEST
K924248 ACCUTEX SLE LATEX TEST
K912716 J&S IRON REAGENTS
Search all 18 clearances from J.S. MEDICAL ASSOC. →