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

RAYDEN MEDICAL MINI PULSE VOLUME RECORD

K Number: K833155 · Decision Jan 26, 1984
Classifications
1
FEI Numbers
69
Registration Numbers
69
Same Product Code
113
Applicant Total
10
Review Days
133

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
RAYDEN MEDICAL MINI PULSE VOLUME RECORD
K Number
K833155
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
870.2770
Medical Specialty
Cardiovascular
Decision
Substantially Equivalent
Applicant
Burditt & Calkins-Siemens-Elema
Date Received
September 15, 1983
Decision Date
January 26, 1984
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.

View all

Other Clearances by Burditt & Calkins-Siemens-Elema

K Number Device Name
K833519 PULSE GENERATOR MODEL 688
K830344 SIEMENS-ELMA PULSE GENERATOR #718
K823435 MON-A-THERM MYOCARDIAL TEMP. SENSOR
K823591 AMEDA HAND BREAST PUMP
K822239 COAXIAL BIPOLAR PACING ELECTRODE
K821712 INFORMED REMOTE FIELD UNIT MODEL IFM1000
K803111 ERECTAID
K802607 TERPERATUR SENSING DEVICE
K760787 LIBERATOR/STROLLER