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FDA 510(k)

VISTA SINGLE CHIP VIDEO CAMERA

K-Number: K971373 · 1997-05-20

ApplicantVista Medical Technologies, Inc.
Decision Date1997-05-20
Product CodeFET
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VISTA SINGLE CHIP VIDEO CAMERA is the device name listed in this FDA 510(k) record. The listed applicant is Vista Medical Technologies, Inc.. It received FDA 510(k) clearance on 1997-05-20 under 510(k) number K971373. The device is classified under product code FET. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA SINGLE CHIP VIDEO CAMERA?

VISTA SINGLE CHIP VIDEO CAMERA is a medical device that received FDA 510(k) clearance on 1997-05-20. The listed applicant is Vista Medical Technologies, Inc.. The 510(k) number is K971373.

When did VISTA SINGLE CHIP VIDEO CAMERA receive FDA 510(k) clearance?

VISTA SINGLE CHIP VIDEO CAMERA received FDA 510(k) clearance on 1997-05-20, under 510(k) number K971373.

Who is the listed applicant for VISTA SINGLE CHIP VIDEO CAMERA?

The FDA 510(k) record lists Vista Medical Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VISTA SINGLE CHIP VIDEO CAMERA?

The FDA product code for VISTA SINGLE CHIP VIDEO CAMERA is FET.

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Other records listing Vista Medical Technologies, 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.

K021290VISTA VISUALIZATION SYSTEM, MODEL 9000, VISTA VISUALIZATION SYSTEM WITH VOICE ACTIVATION AND PIP, MODEL 9100K020301MODIFICATION TO VISTA STEREOSCOPE SYSTEMK991303VISTA ORPC WITH INFOMATIX INTRAOP SOFTWAREK990635VISTA STEREOSCOPE SYSTEMK973436VISTA HEAD MOUNTED DISPLAYK970217VISTA ILLUMINATION SYSTEM

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Related Devices (Code: FET)

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.

K2620794K Camera Head OLYMPUS CH-S700-08-LBOlympus Medical Systems Corp.K261880FUJIFILM Processor EP-8000;Balloon Controller PB-30;Endoscopy Support Program EW10-VM01Fujifilm CorporationK261260HD Camera Head OLYMPUS CH-S200-08-LBOlympus Medical Systems CorporationK251734ProVee Video Processing Unit (PV-003)Proverum LimitedK250462UL UHD-Clear View 4K Camera System (UL-3Chip 4K)Univlabs Technologies Private LimitedK250204Endoscopic Camera SystemShenzhen Sophway Technology Co., Ltd.

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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