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FDA 510(k)

SURGICAL ASPIRATOR KIT

K-Number: K904010 · 1990-11-21

ApplicantSurgeon Surgical Instrumentation, Inc.
Decision Date1990-11-21
Product CodeLFL
DecisionSubstantially Equivalent

Device Summary

SURGICAL ASPIRATOR KIT is the device name listed in this FDA 510(k) record. The listed applicant is Surgeon Surgical Instrumentation, Inc.. It received FDA 510(k) clearance on 1990-11-21 under 510(k) number K904010. The device is classified under product code LFL. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGICAL ASPIRATOR KIT?

SURGICAL ASPIRATOR KIT is a medical device that received FDA 510(k) clearance on 1990-11-21. The listed applicant is Surgeon Surgical Instrumentation, Inc.. The 510(k) number is K904010.

When did SURGICAL ASPIRATOR KIT receive FDA 510(k) clearance?

SURGICAL ASPIRATOR KIT received FDA 510(k) clearance on 1990-11-21, under 510(k) number K904010.

Who is the listed applicant for SURGICAL ASPIRATOR KIT?

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

What is the FDA product code for SURGICAL ASPIRATOR KIT?

The FDA product code for SURGICAL ASPIRATOR KIT is LFL.

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 Surgeon Surgical Instrumentation, 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.

K954241SURGIN GENISIS PHACOEMULSIFIERK932281VERRES NEEDLEK922038CO2 INSUFFLATION TUBINGK890447HEMORRHAGE OCCLUDORK880543UNI-PORTK881232SURGIN EYE SHIELD

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Related Devices (Code: LFL)

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.

K261448neXus Ultrasonic Surgical Aspirator SystemMisonix, LLCK251162CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences CorporationK242894SanAgile™ Ultrasonic Surgery Advanced Portable Controller (SA10); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD14); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD23); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD36); SanAgile™ Ultrasonic Surgery Advanced Dissector (SASD45)Shanghai Saints Sages Surgical Co., Ltd.K243930Sonopet iQ Ultrasonic Aspirator System (5500-050-000)Stryker InstrumentsK241700Tenex 2nd Generation SystemTrice Medical, Inc.K240493CUSA® Clarity Ultrasonic Surgical Aspirator SystemIntegra LifeSciences Corporation

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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