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

LEADWIRE

K Number: K933603 · Decision Jan 18, 1994
Classifications
1
FEI Numbers
139
Registration Numbers
139
Same Product Code
104
Applicant Total
13
Review Days
175

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Basic Information

Device Name
LEADWIRE
K Number
K933603
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2900
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sentry Medical Products, Inc.
Date Received
July 27, 1993
Decision Date
January 18, 1994
Product Code
DSA
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
DSA Cable, Transducer And Electrode, Patient, (Including Connector)

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Other Clearances by Sentry Medical Products, Inc.

K Number Device Name
K962122 SENTRY RADIOTRANSLUCENT ECG ELECTRODES
K955636 SENTRY DISPOSABLE DISPERSIVE ELECTRODE
K942827 SENTRY INSERTION TRAY
K934000 SENTRY AQUEOUS GEL ECG ELECTRODES
K935098 BABY BOARD
K932704 PATIENT CABLE
K881670 ACCUTEMP PLUS
K881343 DURADERM BUTTERFLY
K851522 DIAGNOSTIC ECG DISPOSABLE ELECTRODE
K853552 SENTRY FLEXIBLE TENS
Search all 13 clearances from Sentry Medical Products, Inc. →