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

HPD HUMIDIFYING CHAMBER

K Number: K864173 · Decision Jan 30, 1987
Classifications
1
FEI Numbers
108
Registration Numbers
108
Same Product Code
220
Applicant Total
6
Review Days
98

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Basic Information

Device Name
HPD HUMIDIFYING CHAMBER
K Number
K864173
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5450
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Hpd Medical, Inc.
Date Received
October 24, 1986
Decision Date
January 30, 1987
Product Code
BTT
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
BTT Humidifier, Respiratory Gas, (Direct Patient Interface)

Similar 510(k) Clearances

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

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Other Clearances by Hpd Medical, Inc.

K Number Device Name
K914994 HPD HEATER BASES
K895795 HPD TUBING CONNECTORS
K885314 HPD STERILE HUMIDIFYING CHAMBER
K841851 HPD HUMIDIFIER WICK
K821957 CATH-LOK