FDA 510(k) FDA class 2 Substantially Equivalent 🇲🇾 Malaysia

MULTIPLE BRAND MALE LATEX CONDOM

K Number: K070937 · Decision Sep 21, 2007
Classifications
1
FEI Numbers
77
Registration Numbers
77
Same Product Code
400
Applicant Total
3
Review Days
170

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Basic Information

Device Name
MULTIPLE BRAND MALE LATEX CONDOM
K Number
K070937
Device Class
FDA class 2
Clearance Type
Abbreviated
Regulation Number
884.5300
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Nulatex Sdn. Bhd.
Date Received
April 4, 2007
Decision Date
September 21, 2007
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

Other 510(k) clearances with the same product code (HIS), ordered by most recent decision date.

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Other Clearances by Nulatex Sdn. Bhd.

K Number Device Name
K132107 MALE LATEX CONDOM
K121241 MALE LATEX CONDOM