Atlas FDA

DEUCE

FDA 510(k) clearance K943244 · decided 1995-09-11

Clearance details

K-number
K943244
Device name
DEUCE
Applicant
Apt Technology, Inc.
Decision
Substantially Equivalent
Date received
1994-07-06
Decision date
1995-09-11
Days to decision
432 days
Clearance type
Traditional
Product code
IQA
Device class
2
Regulation number
890.3725
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Shreve, OH, US
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
DELTATALKER WITH INFRARED (K961306)Prentke Romich Co.1996-06-27
IMPERIUM (K953905)Teledyne Brown Engineering1995-11-21
LIAISON COMPUTER ACCESS & ENVIRONMENTAL CONTROL SYSTEM (K953937)Apt Technology, Inc.1995-10-31
SCANNING DIRECTOR (K944585)Prentke Romich Co.1995-02-21
BEDSIDE BUTLER (K944345)Trac Medical, Inc.1994-10-17
LEARN MODE WATERPROOF PENDANT PANIC BUTTON (K940223)Interactive Technologies, Inc.1994-04-29
INFRA-LINK (K926029)Zygo Industries, Inc.1993-03-26
HILL-ROM PATIENT ENVIRONMENTAL CONTROL SYSTEM (K921528)Hill-Rom, Inc.1992-04-20
TONGUETOUCH KEYPAD AND ZOFCOM CONTROL SYSTEM (K911101)Zofcom, Inc.1991-04-25
HOSPITAL/HOME ENVIRONMENTAL CONTROL SYST/HECS-1 (K902664)Prentke Romich Co.1990-07-25
ENVIRONMENTAL CONTROL UNIT MODEL 7000 (K901028)Baylor Biomedical Services1990-03-13
REMOTE CONTROL SWITCH (K900969)Baylor Biomedical Services1990-03-13

Recalls involving this device

No recalls on record reference this clearance.