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FDA 510(k)

SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F

K-Number: K883346 · 1988-09-26

ApplicantDevices For Vascular Intervention, Inc.
Decision Date1988-09-26
Product CodeLIT
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F is the device name listed in this FDA 510(k) record. The listed applicant is Devices For Vascular Intervention, Inc.. It received FDA 510(k) clearance on 1988-09-26 under 510(k) number K883346. The device is classified under product code LIT. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F?

SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F is a medical device that received FDA 510(k) clearance on 1988-09-26. The listed applicant is Devices For Vascular Intervention, Inc.. The 510(k) number is K883346.

When did SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F receive FDA 510(k) clearance?

SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F received FDA 510(k) clearance on 1988-09-26, under 510(k) number K883346.

Who is the listed applicant for SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F?

The FDA 510(k) record lists Devices For Vascular Intervention, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F?

The FDA product code for SIMPSON PERIPHERAL ATHEROCATH W/ADDIT. SIZE 13F is LIT.

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Other records listing Devices For Vascular Intervention, Inc. as applicant

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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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