FDA 510(k) FDA class 1 Substantially Equivalent 🇨🇦 Canada

MUCOLYSE

K Number: K850300 · Decision Mar 20, 1985
Classifications
1
FEI Numbers
16
Registration Numbers
16
Same Product Code
69
Applicant Total
27
Review Days
57

Basic Information

Device Name
MUCOLYSE
K Number
K850300
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
866.2450
Medical Specialty
Microbiology
Decision
Substantially Equivalent
Applicant
PRO-LAB, INC.
Date Received
January 22, 1985
Decision Date
March 20, 1985
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

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