FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

DISPOSABLE ARTHROSCOPY CANNULA SET

K Number: K813000 · Decision Jan 22, 1982
Classifications
1
FEI Numbers
1140
Registration Numbers
1140
Same Product Code
57
Applicant Total
12
Review Days
88

Basic Information

Device Name
DISPOSABLE ARTHROSCOPY CANNULA SET
K Number
K813000
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
888.4540
Medical Specialty
Orthopedic
Decision
Substantially Equivalent
Applicant
CLINICAL TECHNOLOGY CORP.
Date Received
October 26, 1981
Decision Date
January 22, 1982
Product Code
LXH
Advisory Committee
Orthopedic
Review Advisory Committee
OR
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
LXH Orthopedic Manual Surgical Instrument

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (LXH), ordered by most recent decision date.

View all

Other Clearances by CLINICAL TECHNOLOGY CORP.

K Number Device Name
K925080 TEK-LUBE
K872867 BIOSIGN
K880166 BOVIE ULTRASONIC SURGICAL ASPIRATOR, MODEL ME2000
K872705 BOVIE 400-CT ELECTROSURGICAL GENERATOR (UNIT)
K855138 BOVIE ULTRASONIC SURGICAL SYSTEM
K854231 ELECTROSURGICAL CUTTING & COAGULATION DEVICE/ACCES
K853507 STERI-GRIP
K852986 GLYCO-SEP/ALC TEST KIT FOR SEPARAT OF HEMOGLOBIN
K844565 BOVIE X-10 ELECTROSURGICAL GENERATOR(UNIT)
K841272 SICKLE-STAT HEMOGLOBIN S SCREEN KIT
Search all 12 clearances from CLINICAL TECHNOLOGY CORP. →