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FDA 510(k)

CANNULA, INTRAVENOUS, HEPARINIZED

K-Number: K770511 · 1977-04-29

ApplicantSherwood Medical Industries
Decision Date1977-04-29
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CANNULA, INTRAVENOUS, HEPARINIZED is the device name listed in this FDA 510(k) record. The listed applicant is Sherwood Medical Industries. It received FDA 510(k) clearance on 1977-04-29 under 510(k) number K770511. The device is classified under product code FOZ. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANNULA, INTRAVENOUS, HEPARINIZED?

CANNULA, INTRAVENOUS, HEPARINIZED is a medical device that received FDA 510(k) clearance on 1977-04-29. The listed applicant is Sherwood Medical Industries. The 510(k) number is K770511.

When did CANNULA, INTRAVENOUS, HEPARINIZED receive FDA 510(k) clearance?

CANNULA, INTRAVENOUS, HEPARINIZED received FDA 510(k) clearance on 1977-04-29, under 510(k) number K770511.

Who is the listed applicant for CANNULA, INTRAVENOUS, HEPARINIZED?

The FDA 510(k) record lists Sherwood Medical Industries as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CANNULA, INTRAVENOUS, HEPARINIZED?

The FDA product code for CANNULA, INTRAVENOUS, HEPARINIZED is FOZ.

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Other records listing Sherwood Medical Industries 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.

K801070SHERWOOD DISPOSABLE ENDOMETRIAL SAMPLESK801071LANCER GLUCOSE RATE REAGENT KITK792014LANCER L-INA BUFFER, POLYMER, WASH SOLUK792013LANCER L-INA HUMAN REFERENCE SERUMK782077LANCER ICE CUBEK790523ARGYLE ESOPHAGEAL STETHOSCOPE

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Related Devices (Code: FOZ)

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.

K260432Ruby Intravascular CatheterVenocare, Inc.K260165Unimpregnated Central Venous CatheterSpectrum VascularK261041ClearSafe Closed SystemMedSource Labs, LLCK260539MedSource QuickSafe™ Safety IV Catheter; MedSource PurSafe™ Safety IV CatheterMedSource Labs, LLCK253235Introcan Safety® Deep Access XL IV CatheterB.Braun Medical, Inc.K252137BD Insyte™ IV CatheterBecton Dickinson Infusion Therapy Systems, 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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