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FDA 510(k)

VISTA ILLUMINATION SYSTEM

K-Number: K970217 · 1997-04-02

ApplicantVista Medical Technologies, Inc.
Decision Date1997-04-02
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

VISTA ILLUMINATION SYSTEM 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 1997-04-02 under 510(k) number K970217. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VISTA ILLUMINATION SYSTEM?

VISTA ILLUMINATION SYSTEM is a medical device that received FDA 510(k) clearance on 1997-04-02. The listed applicant is Vista Medical Technologies, Inc.. The 510(k) number is K970217.

When did VISTA ILLUMINATION SYSTEM receive FDA 510(k) clearance?

VISTA ILLUMINATION SYSTEM received FDA 510(k) clearance on 1997-04-02, under 510(k) number K970217.

Who is the listed applicant for VISTA ILLUMINATION SYSTEM?

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 ILLUMINATION SYSTEM?

The FDA product code for VISTA ILLUMINATION SYSTEM is FFS.

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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 DISPLAYK971373VISTA SINGLE CHIP VIDEO CAMERA

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Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, 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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