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FDA 510(k)

ERYTHROCATH INTRAVENOUS CATHETER PLA. U.

K-Number: K801414 · 1980-08-13

ApplicantG.D. Searle and Co.
Decision Date1980-08-13
Product CodeFOZ
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ERYTHROCATH INTRAVENOUS CATHETER PLA. U. is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801414. 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 ERYTHROCATH INTRAVENOUS CATHETER PLA. U.?

ERYTHROCATH INTRAVENOUS CATHETER PLA. U. is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is G.D. Searle and Co.. The 510(k) number is K801414.

When did ERYTHROCATH INTRAVENOUS CATHETER PLA. U. receive FDA 510(k) clearance?

ERYTHROCATH INTRAVENOUS CATHETER PLA. U. received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801414.

Who is the listed applicant for ERYTHROCATH INTRAVENOUS CATHETER PLA. U.?

The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ERYTHROCATH INTRAVENOUS CATHETER PLA. U.?

The FDA product code for ERYTHROCATH INTRAVENOUS CATHETER PLA. U. is FOZ.

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Other records listing G.D. Searle and Co. 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.

K821159IN-LINE OXYGEN MONITORING SYSTEMK811068BYPASS COILK811071VENOUS OXYGEN PROBEK803238INTRAVASCULAR CATHETERK810630SILICONE ELASTOMER COATED LATEX FOLEYK810131ADMINISTRATION SET

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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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