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FDA 510(k)

ENDOSCOPIC VIDEO CAMERA

K-Number: K863800 · 1986-10-14

ApplicantTechnology For Imaging, Inc.
Decision Date1986-10-14
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC VIDEO CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Technology For Imaging, Inc.. It received FDA 510(k) clearance on 1986-10-14 under 510(k) number K863800. The device is classified under product code KQM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC VIDEO CAMERA?

ENDOSCOPIC VIDEO CAMERA is a medical device that received FDA 510(k) clearance on 1986-10-14. The listed applicant is Technology For Imaging, Inc.. The 510(k) number is K863800.

When did ENDOSCOPIC VIDEO CAMERA receive FDA 510(k) clearance?

ENDOSCOPIC VIDEO CAMERA received FDA 510(k) clearance on 1986-10-14, under 510(k) number K863800.

Who is the listed applicant for ENDOSCOPIC VIDEO CAMERA?

The FDA 510(k) record lists Technology For Imaging, 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 KQM.

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.

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Other records listing Technology For Imaging, 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.

K885183ENDOSCOPIC LIGHT SOURCEK873419VIDEO PRINTER SYSTEM

Related Devices (Code: KQM)

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.

K900160ADAPTOR: KAPS CINE TO MOELLER BEAMSPLITTERJedmed Instrument Co.K890826SONY VIDEO GRAPHIC PRINTER UP-850Sony Corp. of AmericaK885042SONY TRINITRON COLOR VIDEO MONITOR PVM-1343MDSony Medical Electronics Co.K882958SONY VIDEO PRINTERS, UP SERIESSony Medical Electronics Co.K882924MEDICAM MC-7 AND RP-7 SURGICAL CAMERASM.P. Video, Inc.K873419VIDEO PRINTER SYSTEMTechnology For Imaging, Inc.

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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