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FDA 510(k)

SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2

K-Number: K020252 · 2002-04-05

Decision Date2002-04-05
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 is the device name listed in this FDA 510(k) record. The listed applicant is Harvest Technologies, Corp.. It received FDA 510(k) clearance on 2002-04-05 under 510(k) number K020252. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2?

SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 is a medical device that received FDA 510(k) clearance on 2002-04-05. The listed applicant is Harvest Technologies, Corp.. The 510(k) number is K020252.

When did SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 receive FDA 510(k) clearance?

SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 received FDA 510(k) clearance on 2002-04-05, under 510(k) number K020252.

Who is the listed applicant for SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2?

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

What is the FDA product code for SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2?

The FDA product code for SMARTJET GRAFTING LIQUID APPLICATOR, MODELS SK/S & LK/2 is FMF.

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.

Other records listing Harvest Technologies, 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.

Related Devices (Code: FMF)

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.

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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