FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

DISPOSABLE JOINT ASPIRATION/INJECTION DIAGNOSTIC KIT

K Number: K945831 · Decision Jan 20, 1995
Classifications
1
FEI Numbers
159
Registration Numbers
159
Same Product Code
109
Applicant Total
14
Review Days
52

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Basic Information

Device Name
DISPOSABLE JOINT ASPIRATION/INJECTION DIAGNOSTIC KIT
K Number
K945831
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
878.4370
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Micromed Development Corp.
Date Received
November 29, 1994
Decision Date
January 20, 1995
Product Code
LRO
Advisory Committee
General, Plastic Surgery
Review Advisory Committee
SU
Third Party
N

Classifications

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

Product Code Device Name
LRO General Surgery Tray

Similar 510(k) Clearances

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Other Clearances by Micromed Development Corp.

K Number Device Name
K945105 POLY/PLATINUM WIRE PISTON
K945242 NERVE MONITOR ELECTRODES/STIMULATOR PROBES
K945104 MICROMED PARTIAL REGULAR AND PARTIAL OFFSET
K945107 POLY-WIRE PISTON
K945108 POLY PISTON
K945106 MICROMED TOTAL REGULAR AND PARTIAL OFFSET
K945438 EDI-BUR MICRODRILL SYSTEMS
K943848 COLLAR BUTTON VENTURI VENT TUBE
K943847 BOBBIN STYLE VENTURI VENT TUBE
K943849 GROMMENT STYLE VENTURI TUBE
Search all 14 clearances from Micromed Development Corp. →