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FDA 510(k)

AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT

K-Number: K883522 · 1988-09-30

ApplicantAmerimed US Corp.
Decision Date1988-09-30
Product CodeLBK
DecisionSubstantially Equivalent

Device Summary

AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT is the device name listed in this FDA 510(k) record. The listed applicant is Amerimed US Corp.. It received FDA 510(k) clearance on 1988-09-30 under 510(k) number K883522. The device is classified under product code LBK. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT?

AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT is a medical device that received FDA 510(k) clearance on 1988-09-30. The listed applicant is Amerimed US Corp.. The 510(k) number is K883522.

When did AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT receive FDA 510(k) clearance?

AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT received FDA 510(k) clearance on 1988-09-30, under 510(k) number K883522.

Who is the listed applicant for AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT?

The FDA 510(k) record lists Amerimed US Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT?

The FDA product code for AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT is LBK.

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 Amerimed US Corp. 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.

K891722LATEX EXAM GLOVES (MFG. SHANGHAI MEHECO)K891437PATIENT EXAMINATION GLOVES (LATEX)K891436PATIENT EXAMINATION GLOVES (LATEX)K890967VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)

Related Devices (Code: LBK)

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.

K972612DISSECTRON PORTABLE UNITSatelecK962952OLYMPUS ULTRASONIC SURGICAL SYSTEM (USU)Olympus Optical, Co.K884412CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.Valleylab, Inc.K884413CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATORValleylab, Inc.K855138BOVIE ULTRASONIC SURGICAL SYSTEMClinical Technology Corp.K853143COOPER LASER SONICS CUSA MODEL 200Cooper Lasersonics, 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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