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FDA 510(k)

PS SERIES

K-Number: K061622 · 2007-03-05

ApplicantPhotonic Optische Gerate Gesmbh & Cokg
Decision Date2007-03-05
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

PS SERIES is the device name listed in this FDA 510(k) record. The listed applicant is Photonic Optische Gerate Gesmbh & Cokg. It received FDA 510(k) clearance on 2007-03-05 under 510(k) number K061622. The device is classified under product code FFS. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PS SERIES?

PS SERIES is a medical device that received FDA 510(k) clearance on 2007-03-05. The listed applicant is Photonic Optische Gerate Gesmbh & Cokg. The 510(k) number is K061622.

When did PS SERIES receive FDA 510(k) clearance?

PS SERIES received FDA 510(k) clearance on 2007-03-05, under 510(k) number K061622.

Who is the listed applicant for PS SERIES?

The FDA 510(k) record lists Photonic Optische Gerate Gesmbh & Cokg as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PS SERIES?

The FDA product code for PS SERIES is FFS.

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Related Devices (Code: FFS)

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.

K072521COOK FIBER OPTIC BUNDLE AND FLEXOR DEFLECTING ACCESS SHEATHCook Urological, Inc.K063309TRU-CABLETruphatek International, Ltd.K061025ACCUTECH ENDOLITE PROBEAccutech Medical Technologies, Inc.K023633SOVIS OPTIQUE'S ENDOSCOPIC CABLESovis OptiqueK001698MICRO LINK ENDOSCOPIC FIBER CABLE, MODEL B1-90159Cogent Light Technologies, Inc.K994084SMITH & NEPHEW XENON LIGHT SOURCES AND ACCESSORIESSmith & Nephew, 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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