FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

LADY'S CARE MAXI PADS

K Number: K933950 · Decision Apr 13, 1994
Classifications
1
FEI Numbers
307
Registration Numbers
307
Same Product Code
135
Applicant Total
2
Review Days
244

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Basic Information

Device Name
LADY'S CARE MAXI PADS
K Number
K933950
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
884.5435
Medical Specialty
Obstetrics/Gynecology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Lady'S Care, Inc.
Date Received
August 12, 1993
Decision Date
April 13, 1994
Product Code
HHD
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
HHD Pad, Menstrual, Unscented

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Other Clearances by Lady'S Care, Inc.

K Number Device Name
K935562 PANTY LINERS