Atlas FDA

DYNATRON 2000

FDA 510(k) clearance K880912 · decided 1988-03-15

Clearance details

K-number
K880912
Device name
DYNATRON 2000
Applicant
Dynatronics Corp.
Decision
Substantially Equivalent
Date received
1988-03-03
Decision date
1988-03-15
Days to decision
12 days
Clearance type
Traditional
Product code
IKE
Device class
1
Regulation number
890.1615
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Salt Lake City, UT, US
Third-party review
No
Expedited review
No

+ Add to Predicate Builder ◉ Watch Dynatronics Corp.

Need this as data, not a web page?

Query all 176,000+ clearances through the Atlas FDA API, or subscribe to weekly change alerts. Self-serve from $29/mo.

Similar devices under this product code

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

RecordFirmDate
SONIC PALPOMETER (K060125)Palpometer Systems, Inc.2006-03-16
PRESSORE MONITOR (K954670)Cleveland Medical Devices, Inc.1995-10-30
THE EQUALIZER (K915369)Advanced Rehabilitative Technology, Inc.1993-03-22
PORTABLE LIMB LOAD MONITOR (BMLLM-100) (K915326)Bar Med Pty , Ltd.1992-10-20
IOWA ORAL PERFORMANCE ISNTRUMENT (K920091)Breakthrough, Inc.1992-05-20
FPL (K915897)Wrm Computers1992-04-07
TALLEY SD.500 SKIN PRESSURE EVALUATOR (K914780)Talley Group, Ltd.1991-12-19
MICRO-EMED-SYSTEM (K902967)Novel Electronics, Inc.1990-09-17
BIO-FEEDBACK LIMB MONITOR TYPE CODE BL-34-1 (K875103)Shield Computers , Ltd.1988-01-20
EMED-F-SYSTEM (K871690)Novel GmbH1987-05-15
PODOSCOPE (K864499)Broadwest Corp.1987-02-04
PODODIGITAL (K864569)Broadwest Corp.1987-02-04

Recalls involving this device

No recalls on record reference this clearance.