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FDA 510(k)

PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE

K-Number: K940391 · 1994-06-08

ApplicantPeregrine Surgical , Ltd.
Decision Date1994-06-08
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE 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 1994-06-08 under 510(k) number K940391. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE?

PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE is a medical device that received FDA 510(k) clearance on 1994-06-08. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K940391.

When did PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE receive FDA 510(k) clearance?

PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE received FDA 510(k) clearance on 1994-06-08, under 510(k) number K940391.

Who is the listed applicant for PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE?

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 PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE?

The FDA product code for PEREGRINE REVERSE CUTTING KNIFE LIGHT PIPE is HQE.

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Related Devices (Code: HQE)

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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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