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FDA 510(k)

PEREGRINE WIDE ANGLE LIGHT PIPE

K-Number: K940393 · 1994-09-02

ApplicantPeregrine Surgical , Ltd.
Decision Date1994-09-02
Product CodeHJM
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE WIDE ANGLE 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 1994-09-02 under 510(k) number K940393. The device is classified under product code HJM. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE WIDE ANGLE LIGHT PIPE?

PEREGRINE WIDE ANGLE LIGHT PIPE is a medical device that received FDA 510(k) clearance on 1994-09-02. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K940393.

When did PEREGRINE WIDE ANGLE LIGHT PIPE receive FDA 510(k) clearance?

PEREGRINE WIDE ANGLE LIGHT PIPE received FDA 510(k) clearance on 1994-09-02, under 510(k) number K940393.

Who is the listed applicant for PEREGRINE WIDE ANGLE 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 WIDE ANGLE LIGHT PIPE?

The FDA product code for PEREGRINE WIDE ANGLE LIGHT PIPE is HJM.

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Other records listing Peregrine Surgical , Ltd. 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.

K132614PEREGRINE CURVED ILLUMINATING LASER PROBEK12299723GA CURVED ILLUMINATING LASER PROBEK122905PEREGRINE 23GA CURVED LASER PROBEK061024PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60K031023PEREGRINE ILLUMINATING LASER PROBE MODEL PD600.10K024061PEREGRINE STRAIGHT LASER PROBE, MODEL PD6000.00

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Related Devices (Code: HJM)

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.

K972506INFINITECH BULLET ENDO ILLUMINATED PICK MANIPULATORInfinitech, Inc.K950529PEREGRINE DIFFUSION LIGHT PIPEPeregrine Surgical , Ltd.K945877WECO ENDOSCOPIC SYSTEMS WITH FIBER OPTIC LIGHTWells Johnson Co.K931072HGM ILLUMINATING/ASPIRATING ENDOOCULAR PROBEHgm, Inc.K933445DPS 100 MULTIPORT ILLUMINATION SYSTEM (MIS)Storz Instrument Co.K934269FIBEROPTIC ILLUMINATED INSTRUMENTSVisitec Co.

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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