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

SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHT

K Number: K133425 · Decision Dec 5, 2013
Classifications
1
FEI Numbers
60
Registration Numbers
60
Same Product Code
28
Applicant Total
2
Review Days
27

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Basic Information

Device Name
SCINTILLANT DUAL BENT TIP SURGICAL LIGHT, SCINTILLANT DUAL STRAIGHT TIP SURGICAL LIGHT
K Number
K133425
Device Class
FDA class 2
Clearance Type
Special
Regulation Number
878.4580
Medical Specialty
General, Plastic Surgery
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
Engineered Medical Solutions Co., LLC
Date Received
November 8, 2013
Decision Date
December 5, 2013
Product Code
FTD
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
FTD Lamp, Surgical

Similar 510(k) Clearances

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Other Clearances by Engineered Medical Solutions Co., LLC

K Number Device Name
K071180 SCINTILLANT SURGICAL LIGHT, MODEL 2644-01-0001