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FDA 510(k)

SUPER PETAL SOFT PLASTIC APPLICATOR TAMP

K-Number: K842618 · 1984-07-26

Decision Date1984-07-26
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SUPER PETAL SOFT PLASTIC APPLICATOR TAMP is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1984-07-26 under 510(k) number K842618. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUPER PETAL SOFT PLASTIC APPLICATOR TAMP?

SUPER PETAL SOFT PLASTIC APPLICATOR TAMP is a medical device that received FDA 510(k) clearance on 1984-07-26. The listed applicant is Tambrands, Inc.. The 510(k) number is K842618.

When did SUPER PETAL SOFT PLASTIC APPLICATOR TAMP receive FDA 510(k) clearance?

SUPER PETAL SOFT PLASTIC APPLICATOR TAMP received FDA 510(k) clearance on 1984-07-26, under 510(k) number K842618.

Who is the listed applicant for SUPER PETAL SOFT PLASTIC APPLICATOR TAMP?

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 PETAL SOFT PLASTIC APPLICATOR TAMP?

The FDA product code for SUPER PETAL SOFT PLASTIC APPLICATOR TAMP is HEB.

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: HEB)

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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