SILASTIC BRAND INTRAVAGINAL TARSETTE
K-Number: K771548 · 1977-11-07
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Device Summary
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.
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
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.
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