FDA 510(k) FDA class 2 Substantially Equivalent 🇨🇦 Canada

INDISCAL DIGITAL MANOMETER

K Number: K102192 · Decision Feb 23, 2011
Classifications
1
FEI Numbers
553
Registration Numbers
553
Same Product Code
738
Applicant Total
28
Review Days
203

Basic Information

Device Name
INDISCAL DIGITAL MANOMETER
K Number
K102192
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5860
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Statement or Summary
Summary
Applicant
BAYLIS MEDICAL CO., INC.
Date Received
August 4, 2010
Decision Date
February 23, 2011
Product Code
FMF
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

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

Product Code Device Name
FMF Syringe, Piston

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