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

ECHOBRIGHT

K Number: K093662 · Decision Jun 24, 2010
Classifications
1
FEI Numbers
81
Registration Numbers
81
Same Product Code
154
Applicant Total
14
Review Days
211

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Basic Information

Device Name
ECHOBRIGHT
K Number
K093662
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5140
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Life-Tech, Inc.
Date Received
November 25, 2009
Decision Date
June 24, 2010
Product Code
CAZ
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAZ Anesthesia Conduction Kit

Similar 510(k) Clearances

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Other Clearances by Life-Tech, Inc.

K Number Device Name
K120234 EZONO 3000
K111355 ECHOBRIGHT
K102813 EZONO 3000
K102007 PROLONG, MODELS PL 18040TC, PL18050TGC, PL18100TGC, PL18150TGC,
K093485 VESISCAN
K082772 STIMPRO, MODELS SP22050, SP20100, SPP19050, SPP19100, SPP19150, SPC19050, SPC19100, SPC19150, SPC18050,SPC18100,SPC18150
K082056 ANORECTAL MANOMETRY SOFTWARE OPTION ARM-1
K082923 PRLONG, MODELS PL50, PL100, PL-40C, PL-50C, PL-100C, PL-150C, PLT-40C, PLT-50C, PLT-100C, PLT-150C
K081864 PROLONG
K073187 PERIPHERAL NERVE BLOCK SUPPORT TRAY
Search all 14 clearances from Life-Tech, Inc. →