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FDA 510(k)

MAXI SHIELDS MENSTRUAL PADS

K-Number: K820287 · 1982-03-05

Decision Date1982-03-05
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MAXI SHIELDS MENSTRUAL 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 1982-03-05 under 510(k) number K820287. 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 MAXI SHIELDS MENSTRUAL PADS?

MAXI SHIELDS MENSTRUAL PADS is a medical device that received FDA 510(k) clearance on 1982-03-05. The listed applicant is I.C.D. Industries, Inc.. The 510(k) number is K820287.

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

MAXI SHIELDS MENSTRUAL PADS received FDA 510(k) clearance on 1982-03-05, under 510(k) number K820287.

Who is the listed applicant for MAXI SHIELDS MENSTRUAL 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 MAXI SHIELDS MENSTRUAL PADS?

The FDA product code for MAXI SHIELDS MENSTRUAL 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

View on FDA Database →

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

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