Atlas FDA

RT-200 COMPUTER INTERFACE

FDA 510(k) clearance K875075 · decided 1988-04-21

Clearance details

K-number
K875075
Device name
RT-200 COMPUTER INTERFACE
Applicant
Timeter Instrument Corp.
Decision
Substantially Equivalent
Date received
1987-12-09
Decision date
1988-04-21
Days to decision
134 days
Clearance type
Traditional
Product code
BXX
Device class
1
Regulation number
868.2620
Medical specialty
Anesthesiology
Advisory committee
Anesthesiology
Location
Lancaster, PA, 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
SINGLE DOSE GAS INJECTOR (K923397)Escalon Medical Trek1992-09-14
UTAH PRESSURE TRANSDUCER CALIBRATOR TRU-CAL (K850029)Utah Medical Products, Inc.1985-04-29
RT-200 CALIBRATION ANALYZER (K822746)Timeter Instrument Corp.1982-10-13
NEEDLE COUNTER-SURE COUNT-DISPOSA-TRAY (K801256)Kleen Test Products1980-06-04
NEEDLE COUNTER-SURE COUNT/30 CT. MAGN. (K801257)Kleen Test Products1980-06-04
NEEDLE COUNTER-SURE COUNT/10 COUNT (K801258)Kleen Test Products1980-06-04
SPIROCAL (K791294)Equilibrated Bio Systems, Inc.1979-08-16
PORTABLE PNEUMATIC CALIBRATOR 65-150 (K780981)Pennwalt Corp.1978-08-02
PERCI (K780838)Micro Tronics Corp.1978-07-17

Recalls involving this device

No recalls on record reference this clearance.