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FDA 510(k)

FIBER OPTIC ENDOILLUMINATION PROBE

K-Number: K982462 · 1998-09-14

ApplicantMicrovision, Inc.
Decision Date1998-09-14
Product CodeFFS
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

FIBER OPTIC ENDOILLUMINATION PROBE is the device name listed in this FDA 510(k) record. The listed applicant is Microvision, Inc.. It received FDA 510(k) clearance on 1998-09-14 under 510(k) number K982462. 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 FIBER OPTIC ENDOILLUMINATION PROBE?

FIBER OPTIC ENDOILLUMINATION PROBE is a medical device that received FDA 510(k) clearance on 1998-09-14. The listed applicant is Microvision, Inc.. The 510(k) number is K982462.

When did FIBER OPTIC ENDOILLUMINATION PROBE receive FDA 510(k) clearance?

FIBER OPTIC ENDOILLUMINATION PROBE received FDA 510(k) clearance on 1998-09-14, under 510(k) number K982462.

Who is the listed applicant for FIBER OPTIC ENDOILLUMINATION PROBE?

The FDA 510(k) record lists Microvision, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for FIBER OPTIC ENDOILLUMINATION PROBE?

The FDA product code for FIBER OPTIC ENDOILLUMINATION PROBE is FFS.

Related Clinical Trials

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.

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Other records listing Microvision, Inc. 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.

K022186SCLERAL PLUGS, 19 AND 20 GAUGEK023481MICROVISION SCLERAL BUCKLING COMPONENTS

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.K061622PS SERIESPhotonic Optische Gerate Gesmbh & CokgK063309TRU-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.

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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