TELESCOPE, RIGID ENDOSCOPE
K-Number: K760177 · 1976-08-30
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Device Summary
Frequently Asked Questions
What is the TELESCOPE, RIGID ENDOSCOPE?
TELESCOPE, RIGID ENDOSCOPE is a medical device that received FDA 510(k) clearance on 1976-08-30. The listed applicant is V. Mueller O.V. Baxter Healthcare Corp.. The 510(k) number is K760177.
When did TELESCOPE, RIGID ENDOSCOPE receive FDA 510(k) clearance?
TELESCOPE, RIGID ENDOSCOPE received FDA 510(k) clearance on 1976-08-30, under 510(k) number K760177.
Who is the listed applicant for TELESCOPE, RIGID ENDOSCOPE?
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 TELESCOPE, RIGID ENDOSCOPE?
The FDA product code for TELESCOPE, RIGID ENDOSCOPE is FBP.
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: FBP)
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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