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FDA 510(k)

PERIKON PCL 90

K-Number: K922294 · 1993-01-28

ApplicantOptikon Oftalmologia Spa
Decision Date1993-01-28
Product CodeHPT
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

PERIKON PCL 90 is the device name listed in this FDA 510(k) record. The listed applicant is Optikon Oftalmologia Spa. It received FDA 510(k) clearance on 1993-01-28 under 510(k) number K922294. The device is classified under product code HPT. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PERIKON PCL 90?

PERIKON PCL 90 is a medical device that received FDA 510(k) clearance on 1993-01-28. The listed applicant is Optikon Oftalmologia Spa. The 510(k) number is K922294.

When did PERIKON PCL 90 receive FDA 510(k) clearance?

PERIKON PCL 90 received FDA 510(k) clearance on 1993-01-28, under 510(k) number K922294.

Who is the listed applicant for PERIKON PCL 90?

The FDA 510(k) record lists Optikon Oftalmologia Spa as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PERIKON PCL 90?

The FDA product code for PERIKON PCL 90 is HPT.

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Related Devices (Code: HPT)

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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.

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