Atlas FDA

SECRETARY

FDA 510(k) clearance K924014 · decided 1993-03-04

Clearance details

K-number
K924014
Device name
SECRETARY
Applicant
Zygo Industries, Inc.
Decision
Substantially Equivalent
Date received
1992-08-11
Decision date
1993-03-04
Days to decision
205 days
Clearance type
Traditional
Product code
ILQ
Device class
2
Regulation number
890.3710
Medical specialty
Physical Medicine
Advisory committee
Physical Medicine
Location
Portland, OR, 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
Noddle(TM) (K162817)Iowa Adaptive Technologies, Inc. Dba Voxello, Inc.2017-01-18
P.A.T. SYSTEM (K943035)Mathews Assoc., Inc.1994-10-04
COMFORT KEYBOARD SYSTEM (K930044)Health Care Keyboard Co., Inc.1994-07-14
LIGHTWRITER (K931855)Zygo Corp.1994-05-10
R & D BATTERIES, INC. PART NUMBER 5113 (K935244)R & D Batteries, Inc.1994-04-19
MLT-2 (K935981)Med Labs, Inc.1994-02-17
LIBERATOR (K925387)Prentke Romich Co.1993-03-29
LIGHT TALKER (K925527)Prentke Romich Co.1993-03-22
SCRIBE (K924030)Zygo Industries, Inc.1993-03-04
PARROT (K924015)Zygo Industries, Inc.1993-03-04
MACAW (K924013)Zygo Industries, Inc.1993-03-04
EEC-1 PACKAGE (K923819)Med Labs, Inc.1992-11-06

Recalls involving this device

No recalls on record reference this clearance.