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FDA 510(k)

SILASTIC BRAND INTRAVAGINAL TARSETTE

K-Number: K771548 · 1977-11-07

Decision Date1977-11-07
Product CodeHHW
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

SILASTIC BRAND INTRAVAGINAL TARSETTE is the device name listed in this FDA 510(k) record. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. It received FDA 510(k) clearance on 1977-11-07 under 510(k) number K771548. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SILASTIC BRAND INTRAVAGINAL TARSETTE?

SILASTIC BRAND INTRAVAGINAL TARSETTE is a medical device that received FDA 510(k) clearance on 1977-11-07. The listed applicant is Dow Corning Corp. Healthcare Industries Materials. The 510(k) number is K771548.

When did SILASTIC BRAND INTRAVAGINAL TARSETTE receive FDA 510(k) clearance?

SILASTIC BRAND INTRAVAGINAL TARSETTE received FDA 510(k) clearance on 1977-11-07, under 510(k) number K771548.

Who is the listed applicant for SILASTIC BRAND INTRAVAGINAL TARSETTE?

The FDA 510(k) record lists Dow Corning Corp. Healthcare Industries Materials as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SILASTIC BRAND INTRAVAGINAL TARSETTE?

The FDA product code for SILASTIC BRAND INTRAVAGINAL TARSETTE is HHW.

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 Dow Corning Corp. Healthcare Industries Materials 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 31 devices →

Related Devices (Code: HHW)

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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