OBTURATOR, VISUAL
K-Number: K760172 · 1976-12-02
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Device Summary
Frequently Asked Questions
What is the OBTURATOR, VISUAL?
OBTURATOR, VISUAL is a medical device that received FDA 510(k) clearance on 1976-12-02. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760172.
When did OBTURATOR, VISUAL receive FDA 510(k) clearance?
OBTURATOR, VISUAL received FDA 510(k) clearance on 1976-12-02, under 510(k) number K760172.
Who is the listed applicant for OBTURATOR, VISUAL?
The FDA 510(k) record lists V. Mueller O.V. Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OBTURATOR, VISUAL?
The FDA product code for OBTURATOR, VISUAL is FEC.
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 V. Mueller O.V. Baxter Healthcare Corp. 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: FEC)
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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