Atlas FDA

NOVAMETRIX PULSE OXIMETER, MODEL 500

FDA 510(k) clearance K853124 · decided 1985-11-06

Clearance details

K-number
K853124
Device name
NOVAMETRIX PULSE OXIMETER, MODEL 500
Applicant
Novametrix Medical Systems, Inc.
Decision
Substantially Equivalent
Date received
1985-07-25
Decision date
1985-11-06
Days to decision
104 days
Clearance type
Traditional
Product code
JOM
Device class
2
Regulation number
870.2780
Medical specialty
Cardiovascular
Advisory committee
Cardiovascular
Location
Wallingford, CT, US
Third-party review
No
Expedited review
No

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Recalls involving this device

No recalls on record reference this clearance.

PMA approvals by this applicant

RecordFirmDate
TCO2M MODEL 818 MONITOR (P810022/S014)Novametrix Medical Systems, Inc.1987-10-09
TCO2M MODEL 818 MONITOR (P810022/S013)Novametrix Medical Systems, Inc.1987-01-29
TCO2M MODEL 818 MONITOR (P810022/S012)Novametrix Medical Systems, Inc.1986-06-05
TCO2M MODEL 818 MONITOR (P810022/S011)Novametrix Medical Systems, Inc.1985-11-21
TCO2M MODEL 818 MONITOR (P810022/S009)Novametrix Medical Systems, Inc.1985-09-03
TCO2M MODEL 818 MONITOR (P810022/S010)Novametrix Medical Systems, Inc.1985-07-01
TCO2M MODEL 818 MONITOR (P810022/S008)Novametrix Medical Systems, Inc.1985-03-11
TCO2M MODEL 818 MONITOR (P810022/S007)Novametrix Medical Systems, Inc.1984-12-04