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FDA 510(k)

ENDOSCOPIC CAMERA TV W/AUDIO

K-Number: K832342 · 1983-09-12

ApplicantKamiya Tsusan Kaisha, Ltd.
Decision Date1983-09-12
Product CodeKQM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC CAMERA TV W/AUDIO is the device name listed in this FDA 510(k) record. The listed applicant is Kamiya Tsusan Kaisha, Ltd.. It received FDA 510(k) clearance on 1983-09-12 under 510(k) number K832342. 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 CAMERA TV W/AUDIO?

ENDOSCOPIC CAMERA TV W/AUDIO is a medical device that received FDA 510(k) clearance on 1983-09-12. The listed applicant is Kamiya Tsusan Kaisha, Ltd.. The 510(k) number is K832342.

When did ENDOSCOPIC CAMERA TV W/AUDIO receive FDA 510(k) clearance?

ENDOSCOPIC CAMERA TV W/AUDIO received FDA 510(k) clearance on 1983-09-12, under 510(k) number K832342.

Who is the listed applicant for ENDOSCOPIC CAMERA TV W/AUDIO?

The FDA 510(k) record lists Kamiya Tsusan Kaisha, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ENDOSCOPIC CAMERA TV W/AUDIO?

The FDA product code for ENDOSCOPIC CAMERA TV W/AUDIO 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 Kamiya Tsusan Kaisha, Ltd. 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.

K863161TABLE, OPERATING ROOM, HYDRAULICK832341ARTHROSCOPE-VARIOUS MODELS FIBEROPTICK832340OPERATING ROOM TABLES HYDRAULIC

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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