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

EXTRA PROTECTION POLYURETHANE CONDOM

K Number: K922688 · Decision May 4, 1995
Classifications
1
FEI Numbers
17
Registration Numbers
17
Same Product Code
22
Applicant Total
8
Review Days
1064

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Basic Information

Device Name
EXTRA PROTECTION POLYURETHANE CONDOM
K Number
K922688
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Apex Medical Technologies, Inc.
Date Received
June 4, 1992
Decision Date
May 4, 1995
Product Code
MOL
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
MOL Condom, Synthetic

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Other Clearances by Apex Medical Technologies, Inc.

K Number Device Name
K112165 RHEA CUP
K060933 SOLACE POST-OPERATIVE PAIN RELIEF INFUSION SYSTEM
K954791 SEMINAL FLUID COLLECTION KIT II
K930313 APEX SPECIMEN BAG
K902936 POLYURETHANE CONDOM
K871358 SENSATIONS BRAND CONDOMS
K874539 HI-TOUCH (TM) BRAND SURGICAL GLOVES