FDA 510(k) FDA class 1 Substantially Equivalent 🇺🇸 United States

HME-10 (TM)

K Number: K903054 · Decision Oct 31, 1990
Classifications
1
FEI Numbers
125
Registration Numbers
125
Same Product Code
72
Applicant Total
5
Review Days
112

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
HME-10 (TM)
K Number
K903054
Device Class
FDA class 1
Clearance Type
Traditional
Regulation Number
868.5375
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Pharma Systems, Inc.
Date Received
July 11, 1990
Decision Date
October 31, 1990
Product Code
BYD
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
BYD Condenser, Heat And Moisture (Artificial Nose)

Similar 510(k) Clearances

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

View all

Other Clearances by Pharma Systems, Inc.

K Number Device Name
K903057 FREEVENT (TM)
K903058 BACT-HME (TM)
K903055 EXTENDED LIFE CIRCUITS
K903056 BACTTRAP