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

THE HILL ADJUSTABLE P.T. MOBILIZATION TABLE

K Number: K952358 · Decision Jun 22, 1995
Classifications
1
FEI Numbers
51
Registration Numbers
51
Same Product Code
101
Applicant Total
17
Review Days
56

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
THE HILL ADJUSTABLE P.T. MOBILIZATION TABLE
K Number
K952358
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
890.3760
Medical Specialty
Physical Medicine
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Hill Laboratories Co.
Date Received
April 27, 1995
Decision Date
June 22, 1995
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

Similar 510(k) Clearances

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

View all

Other Clearances by Hill Laboratories Co.

K Number Device Name
K090250 ELECTRO-LIGHT THERAPY
K083183 AKLARUS PHOTOTHERAPY SYSTEM
K072256 HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM WITH OPTIONAL HANDS-FREE OPERATION, MODEL
K062256 HF54 COMBINATION ULTRASOUND INTERFERENTIAL AND PREMODULATED STIMULATION SYSTEM
K063034 AIR-FLEX WITH AUTO-DISTRACTION
K043239 HEALTHSTAR ELITE
K952357 THE HILL ADJUSTABLE PODIATRY MODEL
K952355 THE HILL ADJUSTABLE 90MD
K942109 THE HILL ADJUSTABLE RATH MECHANICAL TABLE
K942256 THE HILL ADJUSTABLE EXTEND-R TABLE
Search all 17 clearances from Hill Laboratories Co. →