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FDA 510(k)

MODIFIED SUPER MAXITHINS PADS, UNSCENTED

K-Number: K862679 · 1986-08-15

Decision Date1986-08-15
Product CodeHHD
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODIFIED SUPER MAXITHINS PADS, UNSCENTED is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1986-08-15 under 510(k) number K862679. 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 MODIFIED SUPER MAXITHINS PADS, UNSCENTED?

MODIFIED SUPER MAXITHINS PADS, UNSCENTED is a medical device that received FDA 510(k) clearance on 1986-08-15. The listed applicant is Tambrands, Inc.. The 510(k) number is K862679.

When did MODIFIED SUPER MAXITHINS PADS, UNSCENTED receive FDA 510(k) clearance?

MODIFIED SUPER MAXITHINS PADS, UNSCENTED received FDA 510(k) clearance on 1986-08-15, under 510(k) number K862679.

Who is the listed applicant for MODIFIED SUPER MAXITHINS PADS, UNSCENTED?

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 MODIFIED SUPER MAXITHINS PADS, UNSCENTED?

The FDA product code for MODIFIED SUPER MAXITHINS PADS, UNSCENTED 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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