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FDA 510(k)

PISTON SYRINGE & HYPODERMIC NEEDLE

K-Number: K022159 · 2002-11-07

Decision Date2002-11-07
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PISTON SYRINGE & HYPODERMIC NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is International Medsurg Connection. It received FDA 510(k) clearance on 2002-11-07 under 510(k) number K022159. 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 PISTON SYRINGE & HYPODERMIC NEEDLE?

PISTON SYRINGE & HYPODERMIC NEEDLE is a medical device that received FDA 510(k) clearance on 2002-11-07. The listed applicant is International Medsurg Connection. The 510(k) number is K022159.

When did PISTON SYRINGE & HYPODERMIC NEEDLE receive FDA 510(k) clearance?

PISTON SYRINGE & HYPODERMIC NEEDLE received FDA 510(k) clearance on 2002-11-07, under 510(k) number K022159.

Who is the listed applicant for PISTON SYRINGE & HYPODERMIC NEEDLE?

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

What is the FDA product code for PISTON SYRINGE & HYPODERMIC NEEDLE?

The FDA product code for PISTON SYRINGE & HYPODERMIC NEEDLE 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 International Medsurg Connection 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.

View all 11 devices →

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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