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

RADIATION THERAPY TREAT. PLAN. SYS.

K Number: K780278 · Decision Mar 2, 1978
Classifications
1
FEI Numbers
20
Registration Numbers
20
Same Product Code
52
Applicant Total
12
Review Days
13

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Basic Information

Device Name
RADIATION THERAPY TREAT. PLAN. SYS.
K Number
K780278
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.5900
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Pfizer Medical Systems, Inc.
Date Received
February 17, 1978
Decision Date
March 2, 1978
Product Code
JAD
Advisory Committee
Radiology
Review Advisory Committee
RA
Third Party
N

Classifications

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

Product Code Device Name
JAD System, Therapeutic, X-Ray

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Other Clearances by Pfizer Medical Systems, Inc.

K Number Device Name
K803032 PFIZER PZ-SLM RAD. THERAPY TRTMT. SIMUL.
K802529 PFIZONIC 100 ULTRASOUND SCANNER
K802528 PFIZONIC 150 ULTRASOUND SCANNER
K802532 PFIZONIC 300 ULTRASOUND SCANNER
K802531 PFIZONIC 200 ULTRASOUND SCANNER
K802530 PFIZONIC 250 ULTRASOUND SCANNER
K801446 PFIZER PZ-CT SCANNER
K800501 PFIZER/AS&E 0450 LOCALIZER
K781752 SCANNER, CT 0450
K772289 SCANNER, CT, 0400
Search all 12 clearances from Pfizer Medical Systems, Inc. →