FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

PROPHYLACTIC

K Number: K772181 · Decision Dec 20, 1977
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
398
Applicant Total
1
Review Days
25

Basic Information

Device Name
PROPHYLACTIC
K Number
K772181
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
OM INDUSTRIES, INC.
Date Received
November 25, 1977
Decision Date
December 20, 1977
Product Code
HIS
Advisory Committee
Obstetrics/Gynecology
Review Advisory Committee
OB
Third Party
N

Classifications

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

Product Code Device Name
HIS Condom

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