FDA 510(k)

NEEDLE-GRABBER

K-Number: K923840 · 1993-07-13

Decision Date1993-07-13

Product CodeGDF

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

NEEDLE-GRABBER is the device name listed in this FDA 510(k) record. The listed applicant is Guardian Angel Products, Inc.. It received FDA 510(k) clearance on 1993-07-13 under 510(k) number K923840. The device is classified under product code GDF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NEEDLE-GRABBER?

NEEDLE-GRABBER is a medical device that received FDA 510(k) clearance on 1993-07-13. The listed applicant is Guardian Angel Products, Inc.. The 510(k) number is K923840.

When did NEEDLE-GRABBER receive FDA 510(k) clearance?

NEEDLE-GRABBER received FDA 510(k) clearance on 1993-07-13, under 510(k) number K923840.

Who is the listed applicant for NEEDLE-GRABBER?

The FDA 510(k) record lists Guardian Angel Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NEEDLE-GRABBER?

The FDA product code for NEEDLE-GRABBER is GDF.

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Other records listing Guardian Angel Products, Inc. as applicant

K030547MODIFICATION TO ZAP GUARD DEFIBRILLATOR TEST PROBE K923835THE ELEVENTH FINGER K910687GUARDIAN GEL, SURGEON'S GLOVING CREAM K896985ZAP-GUARD

Related Devices (Code: GDF)

K031173NEEDLETECH GUIDEWIRE INTRODUCER NEEDLE, MODELS 40021, 40069, 40053, 40042 & 40013Needle Tech Products, Inc.K950311GLOBAL MEDICAL PRODUCTS BREST LESION LOCALIZATION NEEDLE WITH STIFFENED WIREGlobal Medical Products, Ltd.K950007SURGICAL INSTRUMENT GUIDEUnited States Surgical, A Division of Tyco Healthc K945124BREAST LESION LOCALIZATION NEEDLEPromex, Inc.K944942BREAST LESION LOCALIZATION NEEDLEPromedical , Ltd.K935538BAUER TEMNO COAXIAL NEEDLEBauer Medical, Inc.

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.