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FDA 510(k)

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing

K-Number: K210996 · 2021-04-23

Decision Date2021-04-23
Product CodeNRY
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing is a medical device manufactured by Imperative Care, Inc.. It received FDA 510(k) clearance on 2021-04-23 under approval number K210996. The device is classified under product code NRY. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing?

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing is a medical device that received FDA 510(k) clearance on 2021-04-23. It is manufactured by Imperative Care, Inc.. The 510(k) number is K210996.

When was ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing approved by the FDA?

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing received FDA 510(k) clearance on 2021-04-23, under approval number K210996.

What company makes ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing?

ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing is manufactured by Imperative Care, Inc..

What is the FDA product code for ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing?

The FDA product code for ZOOM (71, 55, 45, 35) Reperfusion Catheters; ZOOM Aspiration Tubing is NRY.

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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.