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FDA 510(k)

ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE

K-Number: K926242 · 1993-10-15

ApplicantO.R. Concepts, Inc.
Decision Date1993-10-15
Product CodeGEI
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Concepts, Inc.. It received FDA 510(k) clearance on 1993-10-15 under 510(k) number K926242. The device is classified under product code GEI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE?

ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE is a medical device that received FDA 510(k) clearance on 1993-10-15. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K926242.

When did ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE receive FDA 510(k) clearance?

ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE received FDA 510(k) clearance on 1993-10-15, under 510(k) number K926242.

Who is the listed applicant for ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE?

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

What is the FDA product code for ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE?

The FDA product code for ORC ENDOSCOPIC MONOPOLAR ELECTROSURGICAL PROBE is GEI.

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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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