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FDA 510(k)

PEREGRINE PIC MINIPULATOR

K-Number: K940392 · 1994-08-23

ApplicantPeregrine Surgical , Ltd.
Decision Date1994-08-23
Product CodeKYG
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE PIC MINIPULATOR 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 1994-08-23 under 510(k) number K940392. The device is classified under product code KYG. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE PIC MINIPULATOR?

PEREGRINE PIC MINIPULATOR is a medical device that received FDA 510(k) clearance on 1994-08-23. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K940392.

When did PEREGRINE PIC MINIPULATOR receive FDA 510(k) clearance?

PEREGRINE PIC MINIPULATOR received FDA 510(k) clearance on 1994-08-23, under 510(k) number K940392.

Who is the listed applicant for PEREGRINE PIC MINIPULATOR?

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 PIC MINIPULATOR?

The FDA product code for PEREGRINE PIC MINIPULATOR is KYG.

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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: KYG)

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.

K010353MED-LOGICS DISPOSABLE ALK TUBINGMed-Logics, Inc.K003036TURBO-FLOW INFUSION CANNULA 19 GAGE,20 GAGE,23 GAGE, 25 GAGE, MODEL 101019,101020,101023,101025Retinalabs.ComK993591BLADEWORKS DISPOSABLE ALK TUBINGBlade Works, Inc.K981116SOVEREIGN CATARACT EXTRACTION SYSTEMAllergan, Inc.K980647EYE IRRIGATOR MODEL #2020Eye-Deal Ocular Safety Products, Inc.K974561MOISTAIR FLUID AIR TUBING SETAmerican Medical Devices, Inc.

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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