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FDA 510(k)

V*S*R(TM) SCOPE

K-Number: K895545 · 1989-11-15

ApplicantVsr Enterprises Corp.
Decision Date1989-11-15
Product CodeLDE
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

V*S*R(TM) SCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Vsr Enterprises Corp.. It received FDA 510(k) clearance on 1989-11-15 under 510(k) number K895545. The device is classified under product code LDE. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V*S*R(TM) SCOPE?

V*S*R(TM) SCOPE is a medical device that received FDA 510(k) clearance on 1989-11-15. The listed applicant is Vsr Enterprises Corp.. The 510(k) number is K895545.

When did V*S*R(TM) SCOPE receive FDA 510(k) clearance?

V*S*R(TM) SCOPE received FDA 510(k) clearance on 1989-11-15, under 510(k) number K895545.

Who is the listed applicant for V*S*R(TM) SCOPE?

The FDA 510(k) record lists Vsr Enterprises Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V*S*R(TM) SCOPE?

The FDA product code for V*S*R(TM) SCOPE is LDE.

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Related Devices (Code: LDE)

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.

K945082CYPRESS MEDICAL PRODUCTS STETHOSCOPECypress Medical Products, Ltd.K944337VARIOUS STETHOSCOPESRud Riester GmbH & CO KGK940578MANUAL STETOSCOPEBhs Intl., Inc.K935944PROSCOPES AND ADSCOPESAmerican Diagnostic Corp.K923327STETHOSCOPE COVERAnup Chakraborty Co.K924095TIMEOSCOPE AND FLEXISCOPEStethoscopes of America, 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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