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FDA 510(k)

IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT)

K-Number: K070354 · 2007-10-05

ApplicantInternational Medical Development, Inc.
Decision Date2007-10-05
Product CodeBSP
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) is the device name listed in this FDA 510(k) record. The listed applicant is International Medical Development, Inc.. It received FDA 510(k) clearance on 2007-10-05 under 510(k) number K070354. The device is classified under product code BSP. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT)?

IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) is a medical device that received FDA 510(k) clearance on 2007-10-05. The listed applicant is International Medical Development, Inc.. The 510(k) number is K070354.

When did IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) receive FDA 510(k) clearance?

IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) received FDA 510(k) clearance on 2007-10-05, under 510(k) number K070354.

Who is the listed applicant for IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT)?

The FDA 510(k) record lists International Medical Development, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT)?

The FDA product code for IMD'S ANESTHESIA NEEDLES (TUOHY, QUINCKE AND PENCIL POINT) is BSP.

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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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