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FDA 510(k)

MULTIPLE MANUAL SURGICAL INSTRUMENTS

K-Number: K832686 · 1983-10-14

ApplicantHirata Sangyo Co. USA, Inc.
Decision Date1983-10-14
Product CodeHTO
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

MULTIPLE MANUAL SURGICAL INSTRUMENTS is the device name listed in this FDA 510(k) record. The listed applicant is Hirata Sangyo Co. USA, Inc.. It received FDA 510(k) clearance on 1983-10-14 under 510(k) number K832686. The device is classified under product code HTO. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTIPLE MANUAL SURGICAL INSTRUMENTS?

MULTIPLE MANUAL SURGICAL INSTRUMENTS is a medical device that received FDA 510(k) clearance on 1983-10-14. The listed applicant is Hirata Sangyo Co. USA, Inc.. The 510(k) number is K832686.

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

MULTIPLE MANUAL SURGICAL INSTRUMENTS received FDA 510(k) clearance on 1983-10-14, under 510(k) number K832686.

Who is the listed applicant for MULTIPLE MANUAL SURGICAL INSTRUMENTS?

The FDA 510(k) record lists Hirata Sangyo Co. USA, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MULTIPLE MANUAL SURGICAL INSTRUMENTS?

The FDA product code for MULTIPLE MANUAL SURGICAL INSTRUMENTS is HTO.

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Other records listing Hirata Sangyo Co. USA, 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.

K864106SR-MODEL 230 (MODIFICATION)K842289SR- MODEL 230K833541SURGICAL INSTRUMENTK833542SURGICAL INSTRUMENTK831583GP-303K821989NON-STETHO 7, UM-15TP

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Related Devices (Code: HTO)

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.

K111437SYNTHES RIA SYSTEM (EXPANDED INDICATIONS)Synthes (USA) Products, LLCK042899SYNTHES (USA) RIA SYSTEM - EXPANDED INDICATIONSSynthes (Usa)K013527MODIFICATION TO SYNTHES (USA) REAMER IRRIGATOR ASPIRATOR (RIA) SYSTEMSynthes (Usa)K993335SYNTHES REAMER/IRRIGATOR/ASPIRATOR (RIA) SYSTEMSynthes (Usa)K954915FLEXIBLE INTRAMEDULLARY REAMERZimmer, Inc.K903248COMBINATION REAMEROnyx Medical Corp.

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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