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FDA 510(k)

BURRON VENTED NEEDLE

K-Number: K790472 · 1979-03-26

ApplicantNational Patent Development Corp.
Decision Date1979-03-26
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

BURRON VENTED NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is National Patent Development Corp.. It received FDA 510(k) clearance on 1979-03-26 under 510(k) number K790472. 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 BURRON VENTED NEEDLE?

BURRON VENTED NEEDLE is a medical device that received FDA 510(k) clearance on 1979-03-26. The listed applicant is National Patent Development Corp.. The 510(k) number is K790472.

When did BURRON VENTED NEEDLE receive FDA 510(k) clearance?

BURRON VENTED NEEDLE received FDA 510(k) clearance on 1979-03-26, under 510(k) number K790472.

Who is the listed applicant for BURRON VENTED NEEDLE?

The FDA 510(k) record lists National Patent Development Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BURRON VENTED NEEDLE?

The FDA product code for BURRON VENTED NEEDLE is GAA.

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Other records listing National Patent Development Corp. as applicant

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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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