Atlas FDA

ACCELOGRAPH

FDA 510(k) clearance K870619 · decided 1987-03-16

Clearance details

K-number
K870619
Device name
ACCELOGRAPH
Applicant
Biometer Intl. A/S
Decision
Substantially Equivalent
Date received
1987-02-12
Decision date
1987-03-16
Days to decision
32 days
Clearance type
Traditional
Product code
BXN
Device class
2
Regulation number
868.2775
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Denmark, DK
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
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STIMPOD ST2-3010 NERVE STIMULATOR (K140853)Xavant Technology (Pty), Ltd.2014-11-06
EASYMED PERIPHERAL NERVE STIMULATOR-SUNSTIN (K121743)Sunmed, LLC2013-03-28
MYOGUIDE SYSTEM MODEL 8008 (K111985)Intronix Technologies Corp.2011-12-30
STIMTRODE SINGLE USE NERVE STIMULATOR (K110118)Xavant Technology (Pty), Ltd.2011-02-17
STIMPOD NMS450 NERVE STIMULATOR (K102084)Xavant Technology (Pty), Ltd.2010-12-16
STIMPOD MODEL NMS-400 NERVE STIMULATOR (K093591)Xavant Technology (Pty), Ltd.2009-12-03
ASCEND (K091155)Neurometrix, Inc.2009-09-03
XPOD/XMAP NERVE STIMULATOR (K072092)Xavant Technology (Pty), Ltd.2007-11-15

Recalls involving this device

No recalls on record reference this clearance.