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

BOMED-CDM

K Number: K853706 · Decision Apr 14, 1986
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
8
Review Days
222

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Basic Information

Device Name
BOMED-CDM
K Number
K853706
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Bomed Medical Mfr., Ltd.
Date Received
September 4, 1985
Decision Date
April 14, 1986
Product Code
DSB
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
DSB Plethysmograph, Impedance

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (DSB), ordered by most recent decision date.

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Other Clearances by Bomed Medical Mfr., Ltd.

K Number Device Name
K853705 BOMED-EEA
K831422 BIOFLOW
K831421 BOMED BIOCON
K830792 PULSETTE 110 TRANSCUTANEOUS ELEC-NERVE
K813020 BOMED-NCCOM
K811999 BO MED BIA
K810064 PULSARII, HIGH VOLT. GALVANIC MUSC. STIM