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FDA 510(k)

ORC ENDOSCOPIC INSTRUMENT HOLDER

K-Number: K930399 · 1993-02-17

ApplicantO.R. Concepts, Inc.
Decision Date1993-02-17
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ORC ENDOSCOPIC INSTRUMENT HOLDER 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 1993-02-17 under 510(k) number K930399. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORC ENDOSCOPIC INSTRUMENT HOLDER?

ORC ENDOSCOPIC INSTRUMENT HOLDER is a medical device that received FDA 510(k) clearance on 1993-02-17. The listed applicant is O.R. Concepts, Inc.. The 510(k) number is K930399.

When did ORC ENDOSCOPIC INSTRUMENT HOLDER receive FDA 510(k) clearance?

ORC ENDOSCOPIC INSTRUMENT HOLDER received FDA 510(k) clearance on 1993-02-17, under 510(k) number K930399.

Who is the listed applicant for ORC ENDOSCOPIC INSTRUMENT HOLDER?

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 INSTRUMENT HOLDER?

The FDA product code for ORC ENDOSCOPIC INSTRUMENT HOLDER is MDM.

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Other records listing O.R. Concepts, Inc. as applicant

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Related Devices (Code: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, 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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