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FDA 510(k)

SANPOINT MENSTRUAL TAMPON

K-Number: K961926 · 1996-07-15

ApplicantSanpoint AB
Decision Date1996-07-15
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SANPOINT MENSTRUAL TAMPON is the device name listed in this FDA 510(k) record. The listed applicant is Sanpoint AB. It received FDA 510(k) clearance on 1996-07-15 under 510(k) number K961926. 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 SANPOINT MENSTRUAL TAMPON?

SANPOINT MENSTRUAL TAMPON is a medical device that received FDA 510(k) clearance on 1996-07-15. The listed applicant is Sanpoint AB. The 510(k) number is K961926.

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

SANPOINT MENSTRUAL TAMPON received FDA 510(k) clearance on 1996-07-15, under 510(k) number K961926.

Who is the listed applicant for SANPOINT MENSTRUAL TAMPON?

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

What is the FDA product code for SANPOINT MENSTRUAL TAMPON?

The FDA product code for SANPOINT MENSTRUAL 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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