MINI-UB ENDOSCOPES
K-Number: K941230 · 1994-06-17
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Device Summary
Frequently Asked Questions
What is the MINI-UB ENDOSCOPES?
MINI-UB ENDOSCOPES is a medical device that received FDA 510(k) clearance on 1994-06-17. The listed applicant is Candela Laser Corp.. The 510(k) number is K941230.
When did MINI-UB ENDOSCOPES receive FDA 510(k) clearance?
MINI-UB ENDOSCOPES received FDA 510(k) clearance on 1994-06-17, under 510(k) number K941230.
Who is the listed applicant for MINI-UB ENDOSCOPES?
The FDA 510(k) record lists Candela Laser Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MINI-UB ENDOSCOPES?
The FDA product code for MINI-UB ENDOSCOPES is ODF.
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 Candela Laser 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: ODF)
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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