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FDA 510(k)

UNSCENTED MENSTRUAL PADS-MAXI PADS

K-Number: K813251 · 1981-12-14

Decision Date1981-12-14
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

UNSCENTED MENSTRUAL PADS-MAXI PADS is the device name listed in this FDA 510(k) record. The listed applicant is I.C.D. Industries, Inc.. It received FDA 510(k) clearance on 1981-12-14 under 510(k) number K813251. 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 UNSCENTED MENSTRUAL PADS-MAXI PADS?

UNSCENTED MENSTRUAL PADS-MAXI PADS is a medical device that received FDA 510(k) clearance on 1981-12-14. The listed applicant is I.C.D. Industries, Inc.. The 510(k) number is K813251.

When did UNSCENTED MENSTRUAL PADS-MAXI PADS receive FDA 510(k) clearance?

UNSCENTED MENSTRUAL PADS-MAXI PADS received FDA 510(k) clearance on 1981-12-14, under 510(k) number K813251.

Who is the listed applicant for UNSCENTED MENSTRUAL PADS-MAXI PADS?

The FDA 510(k) record lists I.C.D. Industries, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for UNSCENTED MENSTRUAL PADS-MAXI PADS?

The FDA product code for UNSCENTED MENSTRUAL PADS-MAXI PADS 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.

Other records listing I.C.D. Industries, 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.

View all 9 devices →

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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