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FDA 510(k)

CANAL FINDER

K-Number: K850294 · 1985-06-04

ApplicantRoseburg SA
Decision Date1985-06-04
Product CodeEGS
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CANAL FINDER is the device name listed in this FDA 510(k) record. The listed applicant is Roseburg SA. It received FDA 510(k) clearance on 1985-06-04 under 510(k) number K850294. The device is classified under product code EGS. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CANAL FINDER?

CANAL FINDER is a medical device that received FDA 510(k) clearance on 1985-06-04. The listed applicant is Roseburg SA. The 510(k) number is K850294.

When did CANAL FINDER receive FDA 510(k) clearance?

CANAL FINDER received FDA 510(k) clearance on 1985-06-04, under 510(k) number K850294.

Who is the listed applicant for CANAL FINDER?

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

What is the FDA product code for CANAL FINDER?

The FDA product code for CANAL FINDER is EGS.

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Other records listing Roseburg SA 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.

K931155STAPLE, FIXATION BONE; SCREW FIXATION BONEK890081CALIUS-ISABEL CANOVAS SUNGLASSESK885275ASSENAT-BLESCHET SUNGLASSESK882392BURNET LABORATOIRE PHARMACEUTIQUE SURGICAL GLOVESK872715UNIVERSAL INSTRUMENTATION(CD) FOR SPINAL SURGERYK874317POIRIER KID-ROLLER MANUAL WHEELCHAIR

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Related Devices (Code: EGS)

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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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