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FDA 510(k)

KINETIC CANNULA

K-Number: K012042 · 2001-09-20

ApplicantReliance Medical Corp.
Decision Date2001-09-20
Product CodeQPB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KINETIC CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Reliance Medical Corp.. It received FDA 510(k) clearance on 2001-09-20 under 510(k) number K012042. The device is classified under product code QPB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KINETIC CANNULA?

KINETIC CANNULA is a medical device that received FDA 510(k) clearance on 2001-09-20. The listed applicant is Reliance Medical Corp.. The 510(k) number is K012042.

When did KINETIC CANNULA receive FDA 510(k) clearance?

KINETIC CANNULA received FDA 510(k) clearance on 2001-09-20, under 510(k) number K012042.

Who is the listed applicant for KINETIC CANNULA?

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

What is the FDA product code for KINETIC CANNULA?

The FDA product code for KINETIC CANNULA is QPB.

Related Clinical Trials

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.

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Other records listing Reliance Medical Corp. as applicant

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.

K012044BI-PHASIC INFILTRATORK850704RMC ASPIRATOR - VACUUM PUMP

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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.

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