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FDA 510(k)

MICRO VOLUME DOUBLE LINE EXTENSION SET

K-Number: K850061 · 1985-03-27

ApplicantTravenol Laboratories, S.A.
Decision Date1985-03-27
Product CodeFPA
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MICRO VOLUME DOUBLE LINE EXTENSION SET 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 1985-03-27 under 510(k) number K850061. The device is classified under product code FPA. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MICRO VOLUME DOUBLE LINE EXTENSION SET?

MICRO VOLUME DOUBLE LINE EXTENSION SET is a medical device that received FDA 510(k) clearance on 1985-03-27. The listed applicant is Travenol Laboratories, S.A.. The 510(k) number is K850061.

When did MICRO VOLUME DOUBLE LINE EXTENSION SET receive FDA 510(k) clearance?

MICRO VOLUME DOUBLE LINE EXTENSION SET received FDA 510(k) clearance on 1985-03-27, under 510(k) number K850061.

Who is the listed applicant for MICRO VOLUME DOUBLE LINE EXTENSION SET?

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 MICRO VOLUME DOUBLE LINE EXTENSION SET?

The FDA product code for MICRO VOLUME DOUBLE LINE EXTENSION SET is FPA.

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

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Related Devices (Code: FPA)

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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