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

BETA 90/50 MOBILE IMAGING TABLE

K Number: K884531 · Decision Jan 11, 1989
Classifications
1
FEI Numbers
23
Registration Numbers
23
Same Product Code
76
Applicant Total
2
Review Days
75

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Basic Information

Device Name
BETA 90/50 MOBILE IMAGING TABLE
K Number
K884531
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1980
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Beta Medical Products Co.
Date Received
October 28, 1988
Decision Date
January 11, 1989
Product Code
IXR
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
IXR Table, Radiographic, Tilting

Similar 510(k) Clearances

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

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Other Clearances by Beta Medical Products Co.

K Number Device Name
K863083 BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER