ENDOSCOPIC VIDEO CAMERA
K-Number: K932628 · 1993-10-15
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Device Summary
Frequently Asked Questions
What is the ENDOSCOPIC VIDEO CAMERA?
ENDOSCOPIC VIDEO CAMERA is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is Stephen Chakoff, Inc.. The 510(k) number is K932628.
When did ENDOSCOPIC VIDEO CAMERA receive FDA 510(k) clearance?
ENDOSCOPIC VIDEO CAMERA received FDA 510(k) clearance on 1993-10-15, under 510(k) number K932628.
Who is the listed applicant for ENDOSCOPIC VIDEO CAMERA?
The FDA 510(k) record lists Stephen Chakoff, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ENDOSCOPIC VIDEO CAMERA?
The FDA product code for ENDOSCOPIC VIDEO CAMERA is FWF.
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 Stephen Chakoff, 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: FWF)
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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