Atlas FDA

CMS 6000

FDA 510(k) clearance K792380 · decided 1980-01-04

Clearance details

K-number
K792380
Device name
CMS 6000
Applicant
Physio-Control Corp.
Decision
Substantially Equivalent
Date received
1979-11-26
Decision date
1980-01-04
Days to decision
39 days
Clearance type
Traditional
Product code
GYE
Device class
2
Regulation number
882.1855
Medical specialty
Neurology
Advisory committee
Neurology
Location
Mchenry, IL, 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
WIRELESS EEG RECORDING SYSTEM MODEL W32 (K963195)Cme Telemetrix, Inc.1997-07-29
DT-24 TELEPHONIC EEG TRANSMITTER/DR-24 TELEPHONIC EEG RECEIVER (K970659)Telediagnostic Systems, Inc.1997-05-16
MODEL 219 TELEMETRY SYSTEM (K895895)Mennen Medical, Inc.1990-02-22
BMS-2000 MOBILE EEG SYSTEM (K891405)Buckman Co., Inc.1989-08-02
RS-10 TELEPHONIC POLYSOMNOGRAPHY RECEIVER (K885328)Telediagnostic Systems, Inc.1989-03-22
ISO-100 ISOLATION AMPLIFIER (K883947)Telediagnostic Systems, Inc.1988-12-05
DAD 16S, DATA ACQUISTION DEVICE 16 CH. SERIES (K883461)Biohm, Inc.1988-11-30
S-10 TELEPHONIC POLYSOMNOGRAPH (K874257)Telediagnostic Systems, Inc.1987-12-11
M10 EEG MONITOR SCOPE (K871120)Telediagnostic Systems, Inc.1987-05-01
MODAC-XXXX INTENSIVE MONITORING OF EEG (K860128)Grass-Telefactor Product Group1986-03-27
TELEPHONIC RECEIVER R-10 EEG (K833880)Pharmaquest Corp.1983-11-29
TELEPHONE TRANSMITTER T-10 EEG (K833236)Pharmaquest Corp.1983-11-29

Recalls involving this device

No recalls on record reference this clearance.