FDA 510(k) FDA class 2 Substantially Equivalent 🇸🇪 Sweden

CONDOM (RUBBER LATEX) KILROY

K Number: K894533 · Decision Dec 18, 1989
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
5
Review Days
152

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Basic Information

Device Name
CONDOM (RUBBER LATEX) KILROY
K Number
K894533
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Rfsu
Date Received
July 19, 1989
Decision Date
December 18, 1989
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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Other 510(k) clearances with the same product code (HIS), ordered by most recent decision date.

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Other Clearances by Rfsu

K Number Device Name
K902907 MAMBA CONDOM (RUBBER LATEX)
K895894 PROFIL CONDOM (RUBBER LATEX)
K895028 BIRDS'N BEES CONDOMS
K894534 CONDOM (RUBBER LATEX) OKEIDO