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

VOLU-SOL CARNOY FLUID

K Number: K822126 · Decision Aug 5, 1982
Classifications
1
FEI Numbers
5
Registration Numbers
5
Same Product Code
2
Applicant Total
66
Review Days
17

Basic Information

Device Name
VOLU-SOL CARNOY FLUID
K Number
K822126
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
VOLU SOL MEDICAL INDUSTRIES
Date Received
July 19, 1982
Decision Date
August 5, 1982
Product Code
IGM
Advisory Committee
Pathology
Review Advisory Committee
PA
Third Party
N

Classifications

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

Product Code Device Name
IGM Solution, Carnoy'S

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Other Clearances by VOLU SOL MEDICAL INDUSTRIES

K Number Device Name
K822129 VOLU-SOL BOVINS FIXATIVE
K822127 VOLU-SOL ZENKERS FIXATIVE
K822128 VOLU-SOL SINGLE DIFFERENTIAL STAIN
K822038 VOLU-SOL ORANGE G-6(GILLS-MOD
K822035 VOLU-SOL GILLS EA
K822036 VOLU-SOL DECALCIFER
K822037 VOLU-SOL TAP WATER SUBSTITUTE
K812906 ELVI BICLOT 816
K821540 HEMATOXYLIN II
K821533 HEMATOXYLIN I
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