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FDA 510(k)

MANUAL SURGICAL INSTRUMENTS

K-Number: K920263 · 1992-05-06

ApplicantPhoenix Instruments Div.
Decision Date1992-05-06
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MANUAL SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Phoenix Instruments Div.. It received FDA 510(k) clearance on 1992-05-06 under 510(k) number K920263. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MANUAL SURGICAL INSTRUMENTS?

MANUAL SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1992-05-06. The listed applicant is Phoenix Instruments Div.. The 510(k) number is K920263.

When did MANUAL SURGICAL INSTRUMENTS receive FDA 510(k) clearance?

MANUAL SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1992-05-06, under 510(k) number K920263.

Who is the listed applicant for MANUAL SURGICAL INSTRUMENTS?

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

What is the FDA product code for MANUAL SURGICAL INSTRUMENTS?

The FDA product code for MANUAL SURGICAL INSTRUMENTS is KDC.

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Related Devices (Code: KDC)

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.

K943229DISPOSABLE SURGICAL SCISSORS AND FORCEPSY.M.K. International Co., Ltd.K936226SURGIMED BREAST LOCALIZATION NEEDLE WIRE SETMeadox Medicals, Div. Boston Scientific Corp.K920153THERMUFF BAGTechstylesK915064DISPOSABLE CAUTERY ABRASIVE PADAmerican Medical Mfg., Inc.K914960INSTRUMENT ORGANIZERO.R. Concepts, Inc.K912834SHUR-GRIPInman Medical Corp.

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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