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FDA 510(k)

KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)

K-Number: K896605 · 1990-01-04

ApplicantNational-Standard Medical Products
Decision Date1990-01-04
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) is the device name listed in this FDA 510(k) record. The listed applicant is National-Standard Medical Products. It received FDA 510(k) clearance on 1990-01-04 under 510(k) number K896605. 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 KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)?

KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) is a medical device that received FDA 510(k) clearance on 1990-01-04. The listed applicant is National-Standard Medical Products. The 510(k) number is K896605.

When did KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) receive FDA 510(k) clearance?

KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) received FDA 510(k) clearance on 1990-01-04, under 510(k) number K896605.

Who is the listed applicant for KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)?

The FDA 510(k) record lists National-Standard Medical Products as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)?

The FDA product code for KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG) is GAA.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing National-Standard Medical Products 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.

K900822HYDRO-SIL(TM) COATED GUIDEWIRESK896606JACKSON FINE NEEDLE ASPIRATION SYSTEM

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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