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

ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTOR

K Number: K861981 · Decision Aug 25, 1986
Classifications
1
FEI Numbers
11
Registration Numbers
11
Same Product Code
7
Applicant Total
75
Review Days
95

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Basic Information

Device Name
ELECTROCARDIOGRAPH LEAD SWITCHING ADAPTOR
K Number
K861981
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2350
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Vital Signs, Inc.
Date Received
May 22, 1986
Decision Date
August 25, 1986
Product Code
DRW
Advisory Committee
Cardiovascular
Review Advisory Committee
CV
Third Party
N

Classifications

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

Product Code Device Name
DRW Adaptor, Lead Switching, Electrocardiograph

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Other Clearances by Vital Signs, Inc.

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K112902 ENFLOW IV FLUID WARMER
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K030985 BREAS PV 10I CPAP SYSTEM, MODEL PV 10I
K022402 DISPOSABLE PRESSURE MANOMETER
K021315 SURE-LOK
K002454 BREAS HA50 HUMIDIFIER, MODEL HA50
K001553 BREAS PV 100 CPAP SYSTEM
K000441 BODYGUARD
K994044 CLEEN-ABLE
K990412 CUFF-ABLE PLUS
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