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FDA 510(k)

HARVEST GRAFT DELIVERY SYRINGE

K-Number: K043261 · 2005-03-11

ApplicantHarvest Technologies, Corp.
Decision Date2005-03-11
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HARVEST GRAFT DELIVERY SYRINGE 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 2005-03-11 under 510(k) number K043261. 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 HARVEST GRAFT DELIVERY SYRINGE?

HARVEST GRAFT DELIVERY SYRINGE is a medical device that received FDA 510(k) clearance on 2005-03-11. The listed applicant is Harvest Technologies, Corp.. The 510(k) number is K043261.

When did HARVEST GRAFT DELIVERY SYRINGE receive FDA 510(k) clearance?

HARVEST GRAFT DELIVERY SYRINGE received FDA 510(k) clearance on 2005-03-11, under 510(k) number K043261.

Who is the listed applicant for HARVEST GRAFT DELIVERY SYRINGE?

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 HARVEST GRAFT DELIVERY SYRINGE?

The FDA product code for HARVEST GRAFT DELIVERY SYRINGE is FMF.

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Other records listing Harvest Technologies, Corp. as applicant

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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.

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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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