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FDA 510(k)

SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES

K-Number: K910036 · 1991-04-04

ApplicantSurgical Technologies, Inc.
Decision Date1991-04-04
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Technologies, Inc.. It received FDA 510(k) clearance on 1991-04-04 under 510(k) number K910036. 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 SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES?

SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES is a medical device that received FDA 510(k) clearance on 1991-04-04. The listed applicant is Surgical Technologies, Inc.. The 510(k) number is K910036.

When did SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES receive FDA 510(k) clearance?

SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES received FDA 510(k) clearance on 1991-04-04, under 510(k) number K910036.

Who is the listed applicant for SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES?

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

What is the FDA product code for SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES?

The FDA product code for SURG TECH,INC. 30 GAUGE STRAIGHT EXTRUSION NEEDLES is GAA.

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Other records listing Surgical Technologies, Inc. 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.

K941992CYSTOSCOPEK942029ARTHROSCOPEK946136INFINITECH LIGHTED INFUSION CANNULAK952566OSCILFLATORK951918SURGICAL TECHNOLOGIES, INC. SYRINGEK950683ARTHROGRAM TRAY

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Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN 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.

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