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FDA 510(k)

ULTRA THIN MENSTRUAL PAD

K-Number: K921115 · 1993-05-21

ApplicantIcd Products
Decision Date1993-05-21
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

ULTRA THIN MENSTRUAL PAD is the device name listed in this FDA 510(k) record. The listed applicant is Icd Products. It received FDA 510(k) clearance on 1993-05-21 under 510(k) number K921115. 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 ULTRA THIN MENSTRUAL PAD?

ULTRA THIN MENSTRUAL PAD is a medical device that received FDA 510(k) clearance on 1993-05-21. The listed applicant is Icd Products. The 510(k) number is K921115.

When did ULTRA THIN MENSTRUAL PAD receive FDA 510(k) clearance?

ULTRA THIN MENSTRUAL PAD received FDA 510(k) clearance on 1993-05-21, under 510(k) number K921115.

Who is the listed applicant for ULTRA THIN MENSTRUAL PAD?

The FDA 510(k) record lists Icd Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ULTRA THIN MENSTRUAL PAD?

The FDA product code for ULTRA THIN MENSTRUAL PAD is HHD.

Related Clinical Trials

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.

Related Devices (Code: HHD)

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.

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.

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