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FDA 510(k)

IMM HYPODERMIC NEEDLE SET

K-Number: K070801 · 2007-05-24

Decision Date2007-05-24
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

IMM HYPODERMIC NEEDLE SET is the device name listed in this FDA 510(k) record. The listed applicant is Innovative Medical Manufacturing Co.. It received FDA 510(k) clearance on 2007-05-24 under 510(k) number K070801. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMM HYPODERMIC NEEDLE SET?

IMM HYPODERMIC NEEDLE SET is a medical device that received FDA 510(k) clearance on 2007-05-24. The listed applicant is Innovative Medical Manufacturing Co.. The 510(k) number is K070801.

When did IMM HYPODERMIC NEEDLE SET receive FDA 510(k) clearance?

IMM HYPODERMIC NEEDLE SET received FDA 510(k) clearance on 2007-05-24, under 510(k) number K070801.

Who is the listed applicant for IMM HYPODERMIC NEEDLE SET?

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

What is the FDA product code for IMM HYPODERMIC NEEDLE SET?

The FDA product code for IMM HYPODERMIC NEEDLE SET is FPA.

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 Innovative Medical Manufacturing Co. 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: FPA)

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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