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

MONAGHAN'S PRESSURE ALARM

K Number: K821649 · Decision Aug 5, 1982
Classifications
1
FEI Numbers
55
Registration Numbers
55
Same Product Code
77
Applicant Total
33
Review Days
62

Research this 510(k) in seconds

The Research Assistant summarizes clearance history, predicates and product-code trends — and cites every record.

Free to try · every answer cites its records

Basic Information

Device Name
MONAGHAN'S PRESSURE ALARM
K Number
K821649
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.2600
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Monaghan Medical Corp.
Date Received
June 4, 1982
Decision Date
August 5, 1982
Product Code
CAP
Advisory Committee
Anesthesiology
Review Advisory Committee
AN
Third Party
N

Classifications

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

Product Code Device Name
CAP Monitor, Airway Pressure (Includes Gauge And/Or Alarm)

Similar 510(k) Clearances

Other 510(k) clearances with the same product code (CAP), ordered by most recent decision date.

View all

Other Clearances by Monaghan Medical Corp.

K Number Device Name
K123945 STRIVE DUAL ZONE PEAK FLOW METER
K031514 MODIFICATION TO TRUPEAK PEAK FLOW METER
K023097 TRUEZONE PEAK FLOW METER
K012939 AEROVENT II CHC COLLAPSIBLE HOLDING CHAMBER
K991212 MODIFICATION TO TRUZONE PEAK FLOW METER
K964130 AEROGEAR ASTHMA ACTION KIT
K963089 TRUZONE PEAK FLOW METER
K963095 TRUPEAK PEAK FLOW METER
K955234 TRUPEAK PEAK FLOW METER
K955262 TRUZONE PEAK FLOW METER
Search all 33 clearances from Monaghan Medical Corp. →