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

F.A. MOUNTING MEDIUM

K Number: K781388 · Decision Aug 21, 1978
Classifications
1
FEI Numbers
12
Registration Numbers
12
Same Product Code
6
Applicant Total
57
Review Days
11

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Basic Information

Device Name
F.A. MOUNTING MEDIUM
K Number
K781388
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
864.4010
Medical Specialty
Pathology
Decision
Substantially Equivalent
Applicant
Flow Laboratories, Inc.
Date Received
August 10, 1978
Decision Date
August 21, 1978
Product Code
KEQ
Advisory Committee
Pathology
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
KEQ Media, Mounting, Water Soluble

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K861824 GENTAMICIN SULFATE SOLUTION (10MG GENTAMICIN)
K861791 PENICILLIN-STREPTOMYCIN-FUNGIZONE
K860752 GOAT SERUM (29-391-54)
K860762 GAMMA-FREE HORSE SERUM
K850908 TITERTEK MICROITTRATION EQUIP. HANDIWASH 110 12CHA
K844418 TITERTEK MULTISKAN MCC
K844419 TITERTEK MULTISKAN MSS/340
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