Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS

K-Number: K896113 · 1989-12-13

Decision Date1989-12-13
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Tambrands, Inc.. It received FDA 510(k) clearance on 1989-12-13 under 510(k) number K896113. 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 TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS?

TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS is a medical device that received FDA 510(k) clearance on 1989-12-13. The listed applicant is Tambrands, Inc.. The 510(k) number is K896113.

When did TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS receive FDA 510(k) clearance?

TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS received FDA 510(k) clearance on 1989-12-13, under 510(k) number K896113.

Who is the listed applicant for TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS?

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 TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS?

The FDA product code for TAMPON, PETAL SOFT PLASTIC APPLICATOR, SUPER PLUS 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.

View all 70 devices →

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

View on FDA Database →

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

↑