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FDA 510(k)

ARTHROSCOPIC IRRIGATION SETS-2C4030/31

K-Number: K823496 · 1982-12-28

ApplicantTravenol Laboratories, S.A.
Decision Date1982-12-28
Product CodeGBX
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ARTHROSCOPIC IRRIGATION SETS-2C4030/31 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 1982-12-28 under 510(k) number K823496. The device is classified under product code GBX. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ARTHROSCOPIC IRRIGATION SETS-2C4030/31?

ARTHROSCOPIC IRRIGATION SETS-2C4030/31 is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K823496.

When did ARTHROSCOPIC IRRIGATION SETS-2C4030/31 receive FDA 510(k) clearance?

ARTHROSCOPIC IRRIGATION SETS-2C4030/31 received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823496.

Who is the listed applicant for ARTHROSCOPIC IRRIGATION SETS-2C4030/31?

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 ARTHROSCOPIC IRRIGATION SETS-2C4030/31?

The FDA product code for ARTHROSCOPIC IRRIGATION SETS-2C4030/31 is GBX.

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Other records listing Travenol Laboratories, S.A. as applicant

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Related Devices (Code: GBX)

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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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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