510(k) K971437

Device
BIONICARE STIMULATOR SYSTEM. MODEL BIO-1000
Applicant
MURRAY ELECTRONICS
510(k) number
K971437
Product code
NYN  
Decision
Substantially Equivalent (SESE)
Decision date
1997-07-22
Date received
1997-04-18
Regulation
882.5890
Classification name
Stimulator, Electrical, Transcutaneous, For Arthritis
Medical specialty
Neurology
Review panel
Neurology
Device class
2
Clearance type
Traditional
Statement or summary
Summary
Third party reviewed
No

Applicant Contact#

Contact
KENT C HOFFMAN
Address
260 Schilling Cir. Hunt Valley MD US 21031 21031

FDA Registration Numbers#

Source Documents#

510(k) summary PDF

Other 510(k) Records For Product Code NYN  #

510(k), Device, Applicant table
510(k)DeviceApplicantDecision date
K142236BioniCare Hand SystemVision Quest Industries, Inc.2015-03-23
K111557X-FORCESeven Seas Distribtion and Manufacturing, LLC2011-11-10
K073386JOINT STIM, MODEL 1000Pain Management Technologies2008-07-30
K062325RS-4I MUSCLE STIMULATOR FAMILYRs Medical2007-04-13
K052625BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000Bionicare Medical Technologies, Inc.2005-12-05
K030332MODIFICATION TO BIONICARE STIMULATOR SYSTEM, MODEL BIO-1000Bionicare Medical Technologies, Inc.2003-06-06
K983228BIONICARE STIMILATOR SYSTEM, MODEL BIO-1000Murray Electronics1999-03-15

Legacy Summary#

summary

FDA Review#

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