FDA 510(k)

PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13

K-Number: K980530 · 1998-05-12

Decision Date1998-05-12

Product CodeMPA

Advisory CommitteeGU

DecisionSubstantially Equivalent

Device Summary

PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13 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 1998-05-12 under 510(k) number K980530. The device is classified under product code MPA. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13?

PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13 is a medical device that received FDA 510(k) clearance on 1998-05-12. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K980530.

When did PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13 receive FDA 510(k) clearance?

PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13 received FDA 510(k) clearance on 1998-05-12, under 510(k) number K980530.

Who is the listed applicant for PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13?

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 FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13?

The FDA product code for PEREGRINE FIBER OPTIC BIPOLAR STRAIGHT PICK AND ANGLED PICK, MODELS PD100.12 AND PD100.13 is MPA.

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.