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FDA 510(k)

ORS MODEL 6000 ENDOSCOPE HOLDER

K-Number: K051979 · 2005-08-30

ApplicantO.R. Solutions, Inc.
Decision Date2005-08-30
Product CodeOCT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ORS MODEL 6000 ENDOSCOPE HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is O.R. Solutions, Inc.. It received FDA 510(k) clearance on 2005-08-30 under 510(k) number K051979. The device is classified under product code OCT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ORS MODEL 6000 ENDOSCOPE HOLDER?

ORS MODEL 6000 ENDOSCOPE HOLDER is a medical device that received FDA 510(k) clearance on 2005-08-30. The listed applicant is O.R. Solutions, Inc.. The 510(k) number is K051979.

When did ORS MODEL 6000 ENDOSCOPE HOLDER receive FDA 510(k) clearance?

ORS MODEL 6000 ENDOSCOPE HOLDER received FDA 510(k) clearance on 2005-08-30, under 510(k) number K051979.

Who is the listed applicant for ORS MODEL 6000 ENDOSCOPE HOLDER?

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

What is the FDA product code for ORS MODEL 6000 ENDOSCOPE HOLDER?

The FDA product code for ORS MODEL 6000 ENDOSCOPE HOLDER is OCT.

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Other records listing O.R. Solutions, 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.

K0232831075LD HUSH-SLUSHK023282ORS-3000LDK021288ORS-1000LDK021289WARMER 2000LDK960836DMS-9000K953654ORS-111

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Related Devices (Code: OCT)

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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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