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FDA 510(k)

SCOPEJOCKEY

K-Number: K940780 · 1994-05-10

ApplicantFibertech Instruments, Inc.
Decision Date1994-05-10
Product CodeOCU
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

SCOPEJOCKEY is the device name listed in this FDA 510(k) record. The listed applicant is Fibertech Instruments, Inc.. It received FDA 510(k) clearance on 1994-05-10 under 510(k) number K940780. The device is classified under product code OCU. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SCOPEJOCKEY?

SCOPEJOCKEY is a medical device that received FDA 510(k) clearance on 1994-05-10. The listed applicant is Fibertech Instruments, Inc.. The 510(k) number is K940780.

When did SCOPEJOCKEY receive FDA 510(k) clearance?

SCOPEJOCKEY received FDA 510(k) clearance on 1994-05-10, under 510(k) number K940780.

Who is the listed applicant for SCOPEJOCKEY?

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

What is the FDA product code for SCOPEJOCKEY?

The FDA product code for SCOPEJOCKEY is OCU.

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 Fibertech Instruments, 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.

K951713BUTTON LUBRICATOR

Related Devices (Code: OCU)

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.

K202838Andorate Universal Endoscope Tip GuardGa Health Company LimitedK191715Endoscope Tip Protector - Sterile, Endoscope Tip Protector - Non-sterileSTERIS CorporationK191011Scope ProTechMeditech Endoscopy, Ltd.K030684SCOPE GUARD PROTECTIVE SHEATH, MODEL TEL-SHAcmi CorporationK951104ENDOBOOTUnited States Endoscopy Group, Inc.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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