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FDA 510(k)

PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60

K-Number: K061024 · 2006-06-21

ApplicantPeregrine Surgical , Ltd.
Decision Date2006-06-21
Product CodeHQF
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 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 2006-06-21 under 510(k) number K061024. The device is classified under product code HQF. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60?

PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 is a medical device that received FDA 510(k) clearance on 2006-06-21. The listed applicant is Peregrine Surgical , Ltd.. The 510(k) number is K061024.

When did PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 receive FDA 510(k) clearance?

PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 received FDA 510(k) clearance on 2006-06-21, under 510(k) number K061024.

Who is the listed applicant for PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60?

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 SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60?

The FDA product code for PEREGRINE SOFT TIP ASPIRATING LASER PROBE, MODEL PD720.60 is HQF.

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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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