ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3
K-Number: K936257 · 1994-03-24
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Device Summary
Frequently Asked Questions
What is the ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3?
ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 is a medical device that received FDA 510(k) clearance on 1994-03-24. The listed applicant is Mitsubishi Cable America, Inc.. The 510(k) number is K936257.
When did ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 receive FDA 510(k) clearance?
ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 received FDA 510(k) clearance on 1994-03-24, under 510(k) number K936257.
Who is the listed applicant for ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3?
The FDA 510(k) record lists Mitsubishi Cable America, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3?
The FDA product code for ULTRATHIN FLEXIBLE ENDOSCOPE TAS-211/2.3 is EOB.
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 Mitsubishi Cable America, Inc. 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: EOB)
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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