FDA 510(k)

LADY'S CARE MAXI PADS

K-Number: K933950 · 1994-04-13

Decision Date1994-04-13

Product CodeHHD

Advisory CommitteeOB

DecisionSubstantially Equivalent

Device Summary

LADY'S CARE MAXI PADS is the device name listed in this FDA 510(k) record. The listed applicant is Lady'S Care, Inc.. It received FDA 510(k) clearance on 1994-04-13 under 510(k) number K933950. The device is classified under product code HHD. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LADY'S CARE MAXI PADS?

LADY'S CARE MAXI PADS is a medical device that received FDA 510(k) clearance on 1994-04-13. The listed applicant is Lady'S Care, Inc.. The 510(k) number is K933950.

When did LADY'S CARE MAXI PADS receive FDA 510(k) clearance?

LADY'S CARE MAXI PADS received FDA 510(k) clearance on 1994-04-13, under 510(k) number K933950.

Who is the listed applicant for LADY'S CARE MAXI PADS?

The FDA 510(k) record lists Lady'S Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for LADY'S CARE MAXI PADS?

The FDA product code for LADY'S CARE MAXI PADS is HHD.

Other records listing Lady'S Care, Inc. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K935562PANTY LINERS

Related Devices (Code: HHD)

K071827ALWAYS MENSTRUAL PADSProcter & Gamble, Inc.K012629ALWAYS DUETSProcter & Gamble Co.K003843ENVIVE MINIFORMSProcter & Gamble Co.K993870UNSCENTED INTERLABIAL MENSTRUAL PADProcter & Gamble Co.K980395GLADRAGS COTTON MENSTRUAL PADKeepers!, Inc.K953470FLUSHIES FLUSHABLE/BIODEGRADABLE MENSTRUAL PADS/NAPKINS (ULTRA THINS)Mediquip, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.