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FDA 510(k)

SUPER MAXITHINS BODY-SHAPED MAXI PADS

K-Number: K842950 · 1984-08-23

Decision Date1984-08-23
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUPER MAXITHINS BODY-SHAPED MAXI PADS is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1984-08-23 under 510(k) number K842950. 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 SUPER MAXITHINS BODY-SHAPED MAXI PADS?

SUPER MAXITHINS BODY-SHAPED MAXI PADS is a medical device that received FDA 510(k) clearance on 1984-08-23. The listed applicant is Tambrands, Inc.. The 510(k) number is K842950.

When did SUPER MAXITHINS BODY-SHAPED MAXI PADS receive FDA 510(k) clearance?

SUPER MAXITHINS BODY-SHAPED MAXI PADS received FDA 510(k) clearance on 1984-08-23, under 510(k) number K842950.

Who is the listed applicant for SUPER MAXITHINS BODY-SHAPED MAXI PADS?

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

What is the FDA product code for SUPER MAXITHINS BODY-SHAPED MAXI PADS?

The FDA product code for SUPER MAXITHINS BODY-SHAPED 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 Tambrands, 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.

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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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