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FDA 510(k)

ELECATH MULTI-PURPOSE ARTERIAL SURGER

K-Number: K790444 · 1979-06-11

ApplicantElectro-Catheter Corp.
Decision Date1979-06-11
Product CodeGBA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ELECATH MULTI-PURPOSE ARTERIAL SURGER is the device name listed in this FDA 510(k) record. The listed applicant is Electro-Catheter Corp.. It received FDA 510(k) clearance on 1979-06-11 under 510(k) number K790444. The device is classified under product code GBA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ELECATH MULTI-PURPOSE ARTERIAL SURGER?

ELECATH MULTI-PURPOSE ARTERIAL SURGER is a medical device that received FDA 510(k) clearance on 1979-06-11. The listed applicant is Electro-Catheter Corp.. The 510(k) number is K790444.

When did ELECATH MULTI-PURPOSE ARTERIAL SURGER receive FDA 510(k) clearance?

ELECATH MULTI-PURPOSE ARTERIAL SURGER received FDA 510(k) clearance on 1979-06-11, under 510(k) number K790444.

Who is the listed applicant for ELECATH MULTI-PURPOSE ARTERIAL SURGER?

The FDA 510(k) record lists Electro-Catheter Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ELECATH MULTI-PURPOSE ARTERIAL SURGER?

The FDA product code for ELECATH MULTI-PURPOSE ARTERIAL SURGER is GBA.

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 Electro-Catheter Corp. 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.

K934785MULTIPACEK933450CLOSED TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK933451OPEN TIP MULTI-ELECTRODE CATHETER, MODIFICATIONK943257TIP DEFLECTOR (GENESIS)K934787SILICORE SEMI-FLOATERK874154ELECATH(R) TRANSESOPHAGEAL PACING CATHETER

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Related Devices (Code: GBA)

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.

K861877BYRON WORD BARTHOLIAN GLAND CATHETERByron MedicalK802025BALLOON RETENTION CHEST CATHETERLoseff Medical Designers, Ltd.K781772CATHETER, TRANSLUMINAL BALLOONMedi-Tech, Inc.K781665TUBE, LEATHERMAN/IMBRUCENational Catheter Co. Div. Mallinckrodt

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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