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FDA 510(k)

CORMED HUBER POINT NEEDLE

K-Number: K843083 · 1984-09-05

ApplicantCormed, Inc., Sub. C.R.Bard, Inc.
Decision Date1984-09-05
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CORMED HUBER POINT NEEDLE is the device name listed in this FDA 510(k) record. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. It received FDA 510(k) clearance on 1984-09-05 under 510(k) number K843083. 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 CORMED HUBER POINT NEEDLE?

CORMED HUBER POINT NEEDLE is a medical device that received FDA 510(k) clearance on 1984-09-05. The listed applicant is Cormed, Inc., Sub. C.R.Bard, Inc.. The 510(k) number is K843083.

When did CORMED HUBER POINT NEEDLE receive FDA 510(k) clearance?

CORMED HUBER POINT NEEDLE received FDA 510(k) clearance on 1984-09-05, under 510(k) number K843083.

Who is the listed applicant for CORMED HUBER POINT NEEDLE?

The FDA 510(k) record lists Cormed, Inc., Sub. C.R.Bard, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CORMED HUBER POINT NEEDLE?

The FDA product code for CORMED HUBER POINT NEEDLE is GAA.

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Other records listing Cormed, Inc., Sub. C.R.Bard, 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.

K863606BUTTERFLY NON-CORING NEEDLE SETK860432PERCUTANEOUS INTRODUCER KITK854019PORT-GARDK850967STERILE CORMED MEDIPORTK850674CORMED II AMBULATORY INFUSION PUMPK833915VASCULAR ACCESS CATH. REPAIR KIT

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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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