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

TROJAN RIBBED LATEX CONDOMS W/SPERM. MODIFIED

K Number: K901201 · Decision Apr 16, 1990
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
20
Review Days
35

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Basic Information

Device Name
TROJAN RIBBED LATEX CONDOMS W/SPERM. MODIFIED
K Number
K901201
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Applicant
Carter Products
Date Received
March 12, 1990
Decision Date
April 16, 1990
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

Similar 510(k) Clearances

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Other Clearances by Carter Products

K Number Device Name
K955672 TROJAN POLYURETHANE CONDOM (MODIFICATION)
K942697 TROJAN POLYURETHANE CONDOM
K912901 TROJAN (TM-TBD) CONDOM
K904782 ANSWER QUICK AND SIMPLE AT-HOME PREGNANCY TEST
K904273 MAGNUM PLUS LATEX CONDOMS WITH SPERMICIDAL LUB.
K901202 TROJAN NATURALAMB LUBRICATED NATURAL MODIFIED
K901198 TROJAN PLUS 2 LATEX CONDOMS W/SPERMICIDAL MODIFIED
K901193 TROJAN PLUS LUBRI. LATEX CONDOMS (MODIFIED LABEL)
K901197 TROJAN EXTRA STRENGTH LUBRI. CONDOMS MODI. LABEL
K901194 TROJAN RIBBED LUBRI. LATEX CONDOMS MODIFIED LABEL
Search all 20 clearances from Carter Products →