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FDA 510(k)

RADIATION STERILIZED SUCTION CATHETERS

K-Number: K820109 · 1982-01-29

ApplicantTravenol Laboratories, S.A.
Decision Date1982-01-29
Product CodeBSY
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

RADIATION STERILIZED SUCTION CATHETERS 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 1982-01-29 under 510(k) number K820109. The device is classified under product code BSY. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RADIATION STERILIZED SUCTION CATHETERS?

RADIATION STERILIZED SUCTION CATHETERS is a medical device that received FDA 510(k) clearance on 1982-01-29. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K820109.

When did RADIATION STERILIZED SUCTION CATHETERS receive FDA 510(k) clearance?

RADIATION STERILIZED SUCTION CATHETERS received FDA 510(k) clearance on 1982-01-29, under 510(k) number K820109.

Who is the listed applicant for RADIATION STERILIZED SUCTION CATHETERS?

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 RADIATION STERILIZED SUCTION CATHETERS?

The FDA product code for RADIATION STERILIZED SUCTION CATHETERS is BSY.

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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

View all 206 devices →

Related Devices (Code: BSY)

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.

K031997MALLINCKRODT DAR TY-CARE / TY-CARE EXEL CLOSED SUCTION SYSTEMMallinckrodt Dar S.R.L.K992902AMBU HAND POWER SUCTION PUMPAmbu, Inc.K982945DUAL PURPOSE CLOSED CATHETERSpirit Medical Systems, Inc.K981910SUCTION CATHETERNi-Med, Inc.K972258HI-CARE CLOSED SUCTION SYSTEMMallinckrodt MedicalK973199AMSINO SUCTION CATHETERAmsino Intl., 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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