Atlas FDA

AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT

FDA 510(k) clearance K883522 · decided 1988-09-30

Clearance details

K-number
K883522
Device name
AMERIMED ULTRASONIC SURGICAL ASPIRATION KIT
Applicant
Amerimed US Corp.
Decision
Substantially Equivalent
Date received
1988-08-17
Decision date
1988-09-30
Days to decision
44 days
Clearance type
Traditional
Product code
LBK
Device class
U
Medical specialty
Unknown
Advisory committee
Unknown
Location
Denver, CO, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
DISSECTRON PORTABLE UNIT (K972612)Satelec1997-10-08
OLYMPUS ULTRASONIC SURGICAL SYSTEM (USU) (K962952)Olympus Optical, Co.1996-11-29
CUSA SYSTEM 200H ULTRASONIC SURGICAL ASPIRATOR (K884413)Valleylab, Inc.1988-12-02
CUSA SYSTEM 200C,T & M ULTRASONIC SURGICAL ASPIRA. (K884412)Valleylab, Inc.1988-12-02
BOVIE ULTRASONIC SURGICAL SYSTEM (K855138)Clinical Technology Corp.1986-11-10
COOPER LASER SONICS CUSA MODEL 200 (K853143)Cooper Lasersonics, Inc.1985-10-16

Recalls involving this device

No recalls on record reference this clearance.