1
/
of
0
FDA 510(k), K882816, PULSAR EM
FDA 510(k), K882816, PULSAR EM
Regular price
$89.00 USD
Regular price
Sale price
$89.00 USD
Unit price
/
per
510(K) Number: K882816
Device Name: PULSAR EM
Manufacturer: LARRY INMAN
Device Classification Name: Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
Regulation Number: ILX
Classification Product Code: KXA
Date Received: 07/08/1988
Decision Date: 04/27/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Device Name: PULSAR EM
Manufacturer: LARRY INMAN
Device Classification Name: Diathermy, Shortwave, For Use Other Than Applying Therapeutic Deep Heat
Regulation Number: ILX
Classification Product Code: KXA
Date Received: 07/08/1988
Decision Date: 04/27/1989
Decision: Substantially Equivalent (SESE)
Regulation Medical Specialty: Physical Medicine
Couldn't load pickup availability
- Status: Pending Fast-Track Request
- Delivery: Approximately 1 to 2 weeks when the FOIA office is operating at regular capacity
NOTE: This document is not currently in our library. Upon purchase, we will request the document from the FDA FOIA office. Learn more about Fast-Track Requests here.
View full details