FDA 510(k)

14 INCH BULLET POINT NEEDLE

K-Number: K894874 · 1989-09-22

Decision Date1989-09-22

Product CodeGAA

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

14 INCH BULLET POINT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is R. J. Doyle, Inc.. It received FDA 510(k) clearance on 1989-09-22 under 510(k) number K894874. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 14 INCH BULLET POINT NEEDLE?

14 INCH BULLET POINT NEEDLE is a medical device that received FDA 510(k) clearance on 1989-09-22. The listed applicant is R. J. Doyle, Inc.. The 510(k) number is K894874.

When did 14 INCH BULLET POINT NEEDLE receive FDA 510(k) clearance?

14 INCH BULLET POINT NEEDLE received FDA 510(k) clearance on 1989-09-22, under 510(k) number K894874.

Who is the listed applicant for 14 INCH BULLET POINT NEEDLE?

The FDA 510(k) record lists R. J. Doyle, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for 14 INCH BULLET POINT NEEDLE?

The FDA product code for 14 INCH BULLET POINT NEEDLE is GAA.

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Other records listing R. J. Doyle, Inc. as applicant

K89487816GA X 6 BULLET POINT NEEDLE, FLEX STAINLESS STEE K89488120GA X 7-1/2 THREADING BULLET POINT NEEDLE K89488016GA X 14 FOURTEEN LONG LONG BULLET POINT NEEDL K894882INFILTRATION PUMP SYRINGE K89487916GA X 10 MIDDLE SIZE BULLET POINT NEEDLE K89487316 GA X 10 BULLET POINT NEEDLE

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Related Devices (Code: GAA)

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap Technologies K011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/Injectx K983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/Injectx K974741MANAN ACCURA NEEDLEMedical Device Technologies, Inc.

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.