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

ROYAL 1 OXYGEN CONCENTRATOR

K Number: K822301 · Decision Aug 19, 1982
Classifications
1
FEI Numbers
83
Registration Numbers
83
Same Product Code
286
Applicant Total
4
Review Days
16

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Basic Information

Device Name
ROYAL 1 OXYGEN CONCENTRATOR
K Number
K822301
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5440
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Proto-Med, Inc.
Date Received
August 3, 1982
Decision Date
August 19, 1982
Product Code
CAW
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
CAW Generator, Oxygen, Portable

Similar 510(k) Clearances

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

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Other Clearances by Proto-Med, Inc.

K Number Device Name
K844852 THE GENERIC OXYGEN CONCENTRATOR
K820115 EMMETT IUD THREAD RETREIVER
K811761 THE EMMETT IUD THREAD RETRIEVER