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

ELECTRIC TILT TABLE MODEL 9505

K Number: K932239 · Decision Jul 22, 1993
Classifications
1
FEI Numbers
52
Registration Numbers
52
Same Product Code
101
Applicant Total
11
Review Days
76

Basic Information

Device Name
ELECTRIC TILT TABLE MODEL 9505
K Number
K932239
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
BAILEY MFG. CO.
Date Received
May 7, 1993
Decision Date
July 22, 1993
Product Code
INQ
Advisory Committee
Physical Medicine
Review Advisory Committee
PM
Third Party
N

Classifications

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

Product Code Device Name
INQ Table, Powered

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Other Clearances by BAILEY MFG. CO.

K Number Device Name
K932240 MODEL 5200-10,5200-12 HI-LOW ELEC. PARRALLEL BARS
K932236 PRO. HI-LOW TABLE MODEL 9530
K932235 PRO. HI-LOW MAT TABLES #9610-9612 9620-9622
K932241 ECONOMY HI-LOW MAT TABLES/ELECTRIC MODELS
K932232 PROFESSONAL HI-LOW WORK TABLE MODEL 3400
K932233 ECONOMY HI-LOW WORK TABLE (MANUAL) MODEL 3405
K932238 ECO. HI-LOW TREATMENT TABLES VARIOUS MODEL NUMBERS
K932231 ECONOMY HI-LOW MAT TABLE #4110 THRU 4117
K932234 PROFESSIONAL & ECONMY TILT TABLE 9500 9520
K932237 PRO. HI-LOW TREATMENT TABLES MODELS 4050,4070,4090
Search all 11 clearances from BAILEY MFG. CO. →