AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT— 510(k) K883522

Name: FDA 510(k) clearance K883522
Creator: U.S. Food and Drug Administration
Published: 1988-09-30

Substantially Equivalent

Amerimed US Corp.

FDA 510(k) clearance K883522 for AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT, Substantially Equivalent on 1988-09-30. Applicant: Amerimed US Corp.. Device class: Unclassified.

Clearance details

Applicant: Amerimed US Corp.
Product code: Code LBK
Device class: Unclassified
Advisory panel: Unknown
Date received: 1988-08-17
Decision date: 1988-09-30
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Denver, CO, US

Download summary PDF View on FDA.gov ↗

Recent devices under product code LBK

view all

K972612 — DISSECTRON PORTABLE UNIT1997-10-08
K962952 — OLYMPUS ULTRASONIC SURGICAL SYSTEM (USU)1996-11-29
K884412 — CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA.1988-12-02
K884413 — CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR1988-12-02
K855138 — BOVIE ULTRASONIC SURGICAL SYSTEM1986-11-10

More clearances from Amerimed US Corp.

view all

K891722 — LATEX EXAM GLOVES (MFG. SHANGHAI MEHECO)1989-07-14
K891436 — PATIENT EXAMINATION GLOVES (LATEX)1989-05-31
K891437 — PATIENT EXAMINATION GLOVES (LATEX)1989-05-31
K890967 — VINYL EXAMINATION GLOVES (MFG. SALZGITTER MOREX)1989-05-04

Data sourced from openFDA. This site is unofficial and independent of the FDA.