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FDA 510(k)

V.F.I.-VISCOUS FLUID INFUSION TUBING SET

K-Number: K981907 · 1998-08-04

ApplicantPeregrine Surgical , Ltd.
Decision Date1998-08-04
Product CodeMRH
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

V.F.I.-VISCOUS FLUID INFUSION TUBING SET is the device name listed in this FDA 510(k) record. The listed applicant is Peregrine Surgical , Ltd.. It received FDA 510(k) clearance on 1998-08-04 under 510(k) number K981907. The device is classified under product code MRH. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the V.F.I.-VISCOUS FLUID INFUSION TUBING SET?

V.F.I.-VISCOUS FLUID INFUSION TUBING SET is a medical device that received FDA 510(k) clearance on 1998-08-04. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K981907.

When did V.F.I.-VISCOUS FLUID INFUSION TUBING SET receive FDA 510(k) clearance?

V.F.I.-VISCOUS FLUID INFUSION TUBING SET received FDA 510(k) clearance on 1998-08-04, under 510(k) number K981907.

Who is the listed applicant for V.F.I.-VISCOUS FLUID INFUSION TUBING SET?

The FDA 510(k) record lists Peregrine Surgical , Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V.F.I.-VISCOUS FLUID INFUSION TUBING SET?

The FDA product code for V.F.I.-VISCOUS FLUID INFUSION TUBING SET is MRH.

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Related Devices (Code: MRH)

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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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