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FDA 510(k)

YSANPOINT) (MENSTRUAL) DIGITAL TAMPON

K-Number: K962712 · 1996-09-10

Decision Date1996-09-10
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

YSANPOINT) (MENSTRUAL) DIGITAL TAMPON is the device name listed in this FDA 510(k) record. The listed applicant is Talbot S. Lindstrom. It received FDA 510(k) clearance on 1996-09-10 under 510(k) number K962712. 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 YSANPOINT) (MENSTRUAL) DIGITAL TAMPON?

YSANPOINT) (MENSTRUAL) DIGITAL TAMPON is a medical device that received FDA 510(k) clearance on 1996-09-10. The listed applicant is Talbot S. Lindstrom. The 510(k) number is K962712.

When did YSANPOINT) (MENSTRUAL) DIGITAL TAMPON receive FDA 510(k) clearance?

YSANPOINT) (MENSTRUAL) DIGITAL TAMPON received FDA 510(k) clearance on 1996-09-10, under 510(k) number K962712.

Who is the listed applicant for YSANPOINT) (MENSTRUAL) DIGITAL TAMPON?

The FDA 510(k) record lists Talbot S. Lindstrom as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for YSANPOINT) (MENSTRUAL) DIGITAL TAMPON?

The FDA product code for YSANPOINT) (MENSTRUAL) DIGITAL TAMPON 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.

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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