FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

VOLUME CONTROL DEVICE VCD-150

K Number: K780465 · Decision Jun 2, 1978
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
34
Applicant Total
69
Review Days
72

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Basic Information

Device Name
VOLUME CONTROL DEVICE VCD-150
K Number
K780465
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
880.5420
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sorensen Research
Date Received
March 22, 1978
Decision Date
June 2, 1978
Product Code
KZD
Advisory Committee
General Hospital
Review Advisory Committee
HE
Third Party
N

Classifications

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

Product Code Device Name
KZD Infusor, Pressure, For I.V. Bags

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K833096 TRANSDUCER DOME DS106
K832957 FLOW-DIRECTED HEPARIN COATED THERMODIL
K831506 DISP. TRANSDUCER W/MONITORING KIT TRANS
K831939 TALL FLOOR STAND TFS-01
K831505 THORACIC GAUGE #TG-60 -VACUUM REGULATOR
K820706 WATERLESS SEAL & VACUUM REGULATOR
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