FDA 510(k) FDA class 2 Substantially Equivalent 🇺🇸 United States

RS-10 TELEPHONIC POLYSOMNOGRAPHY RECEIVER

K Number: K885328 · Decision Mar 22, 1989
Classifications
1
FEI Numbers
0
Registration Numbers
0
Same Product Code
19
Applicant Total
14
Review Days
84

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Basic Information

Device Name
RS-10 TELEPHONIC POLYSOMNOGRAPHY RECEIVER
K Number
K885328
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
882.1855
Medical Specialty
Neurology
Decision
Substantially Equivalent
Applicant
Telediagnostic Systems, Inc.
Date Received
December 28, 1988
Decision Date
March 22, 1989
Product Code
GYE
Advisory Committee
Neurology
Review Advisory Committee
NE
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
GYE Encephalogram Telemetry System

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Other Clearances by Telediagnostic Systems, Inc.

K Number Device Name
K071661 ALPHAONE BIOFEEDBACK SYSTEM
K022249 NIGHTRON POLYSOMNOGRAPHY SYSTEM
K970659 DT-24 TELEPHONIC EEG TRANSMITTER/DR-24 TELEPHONIC EEG RECEIVER
K904328 VISTA POLYSOMNOGRAPHY COMPUTER SYSTEM
K904222 VISTA GRAPH POLYSOMNOGRAPHY AMPLIFIER
K884891 OC-100 OXIMETER INTERFACE CALIBRATOR
K883947 ISO-100 ISOLATION AMPLIFIER
K874257 S-10 TELEPHONIC POLYSOMNOGRAPH
K871120 M10 EEG MONITOR SCOPE
K810872 EEG TELEPHONE RECEIVER MODEL #AFR-J
Search all 14 clearances from Telediagnostic Systems, Inc. →