FDA 510(k)

PMT VASCULAR CATHETER MODEL NUMBER 3621-1

K-Number: K883313 · 1988-10-04

Decision Date1988-10-04

Product CodeLJS

Advisory CommitteeHO

DecisionSubstantially Equivalent

Device Summary

PMT VASCULAR CATHETER MODEL NUMBER 3621-1 is the device name listed in this FDA 510(k) record. The listed applicant is Pmt Corp.. It received FDA 510(k) clearance on 1988-10-04 under 510(k) number K883313. The device is classified under product code LJS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMT VASCULAR CATHETER MODEL NUMBER 3621-1?

PMT VASCULAR CATHETER MODEL NUMBER 3621-1 is a medical device that received FDA 510(k) clearance on 1988-10-04. The listed applicant is Pmt Corp.. The 510(k) number is K883313.

When did PMT VASCULAR CATHETER MODEL NUMBER 3621-1 receive FDA 510(k) clearance?

PMT VASCULAR CATHETER MODEL NUMBER 3621-1 received FDA 510(k) clearance on 1988-10-04, under 510(k) number K883313.

Who is the listed applicant for PMT VASCULAR CATHETER MODEL NUMBER 3621-1?

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

What is the FDA product code for PMT VASCULAR CATHETER MODEL NUMBER 3621-1?

The FDA product code for PMT VASCULAR CATHETER MODEL NUMBER 3621-1 is LJS.

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Other records listing Pmt Corp. as applicant

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Related Devices (Code: LJS)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.