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

MODEL C2-5000 OVERHEAD TUBE SUPPORT

K Number: K873283 · Decision Sep 10, 1987
Classifications
1
FEI Numbers
34
Registration Numbers
34
Same Product Code
39
Applicant Total
7
Review Days
24

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Basic Information

Device Name
MODEL C2-5000 OVERHEAD TUBE SUPPORT
K Number
K873283
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
892.1770
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Transworld X-Ray Corp.
Date Received
August 17, 1987
Decision Date
September 10, 1987
Product Code
IYB
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
IYB Tube Mount, X-Ray, Diagnostic

Similar 510(k) Clearances

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

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Other Clearances by Transworld X-Ray Corp.

K Number Device Name
K892657 SENSIMAT
K890066 STAR 36
K872980 MAM-CP X-RAY APPARATUS
K872357 TRANSWORLD 360V, MODEL A1-4040
K841923 DCX-100 CHEST UNIT-GL-5000M
K827582 MODIFIED X-RAY TABLE