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

PFIZER PZ-CT SCANNER

K Number: K801446 · Decision Jul 28, 1980
Classifications
1
FEI Numbers
163
Registration Numbers
163
Same Product Code
818
Applicant Total
12
Review Days
38

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Basic Information

Device Name
PFIZER PZ-CT SCANNER
K Number
K801446
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1750
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Pfizer Medical Systems, Inc.
Date Received
June 20, 1980
Decision Date
July 28, 1980
Product Code
JAK
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
JAK System, X-Ray, Tomography, Computed

Similar 510(k) Clearances

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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
K800501 PFIZER/AS&E 0450 LOCALIZER
K781752 SCANNER, CT 0450
K780278 RADIATION THERAPY TREAT. PLAN. SYS.
K772289 SCANNER, CT, 0400
Search all 12 clearances from Pfizer Medical Systems, Inc. →