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FDA 510(k)

ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS

K-Number: K944954 · 1994-11-08

ApplicantUnited Fortune International, Inc.
Decision Date1994-11-08
Product CodeGCJ
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is United Fortune International, Inc.. It received FDA 510(k) clearance on 1994-11-08 under 510(k) number K944954. The device is classified under product code GCJ. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?

ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1994-11-08. The listed applicant is United Fortune International, Inc.. The 510(k) number is K944954.

When did ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1994-11-08, under 510(k) number K944954.

Who is the listed applicant for ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?

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

What is the FDA product code for ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS?

The FDA product code for ENDOSCOPIC REPOSABLE TIP SURGICAL INSTRUMENTS is GCJ.

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 United Fortune International, 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.

K891422PATIENT EXAMINATION GLOVES (LATEX)

Related Devices (Code: GCJ)

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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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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