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FDA 510(k)

CATHETER, CEBTRAL VENOUS, 2N1501

K-Number: K771861 · 1977-11-28

ApplicantTravenol Laboratories, S.A.
Decision Date1977-11-28
Product CodeJCY
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

CATHETER, CEBTRAL VENOUS, 2N1501 is the device name listed in this FDA 510(k) record. The listed applicant is Travenol Laboratories, S.A.. It received FDA 510(k) clearance on 1977-11-28 under 510(k) number K771861. The device is classified under product code JCY. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CATHETER, CEBTRAL VENOUS, 2N1501?

CATHETER, CEBTRAL VENOUS, 2N1501 is a medical device that received FDA 510(k) clearance on 1977-11-28. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K771861.

When did CATHETER, CEBTRAL VENOUS, 2N1501 receive FDA 510(k) clearance?

CATHETER, CEBTRAL VENOUS, 2N1501 received FDA 510(k) clearance on 1977-11-28, under 510(k) number K771861.

Who is the listed applicant for CATHETER, CEBTRAL VENOUS, 2N1501?

The FDA 510(k) record lists Travenol Laboratories, S.A. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CATHETER, CEBTRAL VENOUS, 2N1501?

The FDA product code for CATHETER, CEBTRAL VENOUS, 2N1501 is JCY.

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Other records listing Travenol Laboratories, S.A. 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.

K874181BAXTER BEDSIDE SYSTEMK873894CONTINU-FLO SOLUTION W/CHECK VALVE 2 Y-INJECT SITEK873873RESUBMITTED MICRON TRANSFUSION FILTERK873984AUTOMATIC PERITONEAL DIALYSIS CYCLER SET (5C4437)K872364HEMODIALYSIS (SPS), MODEL 550, CODE 5M1309K872652UPGRADED AUTO PERITONEAL DIALYSIS CYCLER SYSTEM

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Related Devices (Code: JCY)

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.

K863982VAS-CATH PERICARDIOCENTESIS CATHETER, SET & TRAYVas-Cath of Canada , Ltd.K840324SILICONE SUMP DRAIN 20 & 40 FRENCHSuperior Plastic Products Corp.K834615TRIPLE LUMEN INFUSIONCATHETERS-Medical Components, Inc.K831453SILCATH CENTRAL CATHETER TRAY W/18 GAArgon Medical Corp.K831451SILCATH CENTRAL CATHETER TRAY SIZE-Argon Medical Corp.K822096CHEMOTHERAPY INFUSION CATHETERAmerican Heyer Schulte

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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