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FDA 510(k)

JACKSON FINE NEEDLE ASPIRATION SYSTEM

K-Number: K896606 · 1990-01-04

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

Device Summary

JACKSON FINE NEEDLE ASPIRATION SYSTEM 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 K896606. 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 JACKSON FINE NEEDLE ASPIRATION SYSTEM?

JACKSON FINE NEEDLE ASPIRATION SYSTEM 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 K896606.

When did JACKSON FINE NEEDLE ASPIRATION SYSTEM receive FDA 510(k) clearance?

JACKSON FINE NEEDLE ASPIRATION SYSTEM received FDA 510(k) clearance on 1990-01-04, under 510(k) number K896606.

Who is the listed applicant for JACKSON FINE NEEDLE ASPIRATION SYSTEM?

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 JACKSON FINE NEEDLE ASPIRATION SYSTEM?

The FDA product code for JACKSON FINE NEEDLE ASPIRATION SYSTEM 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.

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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 GUIDEWIRESK896605KOPANS STABILIZED NEEDLE ASPIRATION GUIDE (SNAG)

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

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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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