CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)
K-Number: K971584 · 1997-05-23
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Device Summary
Frequently Asked Questions
What is the CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)?
CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES) is a medical device that received FDA 510(k) clearance on 1997-05-23. The listed applicant is Clarus Medical Systems, Inc.. The 510(k) number is K971584.
When did CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES) receive FDA 510(k) clearance?
CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES) received FDA 510(k) clearance on 1997-05-23, under 510(k) number K971584.
Who is the listed applicant for CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)?
The FDA 510(k) record lists Clarus Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES)?
The FDA product code for CLARUS MODEL 2127-900 SERIES ENDOSCOPE ADATER (2127-900 SERIES) is OCV.
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 Clarus Medical Systems, 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: OCV)
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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