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FDA 510(k)

VASCU-CARE ANGIOSCOPE

K-Number: K880927 · 1988-05-16

ApplicantVascu-Care, Inc.
Decision Date1988-05-16
Product CodeDQX
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

VASCU-CARE ANGIOSCOPE is the device name listed in this FDA 510(k) record. The listed applicant is Vascu-Care, Inc.. It received FDA 510(k) clearance on 1988-05-16 under 510(k) number K880927. The device is classified under product code DQX. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the VASCU-CARE ANGIOSCOPE?

VASCU-CARE ANGIOSCOPE is a medical device that received FDA 510(k) clearance on 1988-05-16. The listed applicant is Vascu-Care, Inc.. The 510(k) number is K880927.

When did VASCU-CARE ANGIOSCOPE receive FDA 510(k) clearance?

VASCU-CARE ANGIOSCOPE received FDA 510(k) clearance on 1988-05-16, under 510(k) number K880927.

Who is the listed applicant for VASCU-CARE ANGIOSCOPE?

The FDA 510(k) record lists Vascu-Care, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VASCU-CARE ANGIOSCOPE?

The FDA product code for VASCU-CARE ANGIOSCOPE is DQX.

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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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