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

MODEL 3150-21 QUADRATURE SPINE COIL IN POSITIONER

K Number: K910514 · Decision Mar 19, 1991
Classifications
1
FEI Numbers
146
Registration Numbers
146
Same Product Code
1098
Applicant Total
57
Review Days
42

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
MODEL 3150-21 QUADRATURE SPINE COIL IN POSITIONER
K Number
K910514
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
892.1000
Medical Specialty
Radiology
Decision
Substantially Equivalent
Applicant
Medical Advances, Inc.
Date Received
February 5, 1991
Decision Date
March 19, 1991
Product Code
LNH
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
LNH System, Nuclear Magnetic Resonance Imaging

Similar 510(k) Clearances

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

View all

Other Clearances by Medical Advances, Inc.

K Number Device Name
K023084 MODEL 472GE-128: QUADRATURE LOWER EXTREMITY COIL
K021433 MODEL 415PH-64/42: PHASED ARRAY SHOULDER COIL
K011608 MODEL 235GE-64; MULTI PURPOSE FLEX ARRAY COIL
K010074 MODEL 455GE PHASED ARRAY WRIST COIL
K003685 MODEL 342GE-64 HIGH RESOLUTION BRAIN COIL
K003144 MODEL 205GE-64: PATHWAY MRI CAROTID ARRAY COIL
K000345 MULTI PURPOSE FLEX ARRAY COIL : MODEL 235 SERIES
K991724 QUADRATURE LOWER EXTREMITY COIL, MODEL 473PH-64
K991434 QUADRATURE WRIST COIL, MODEL 445PH-64
K991113 `INEAR WRIST COIL, MODEL 440GE-09
Search all 57 clearances from Medical Advances, Inc. →