510(k) K840817

DISPOSABLE, HYPERBARIC OXYGEN CHAMBER by Hospitak, Inc. — Product Code KPJ

K840817 is an FDA 510(k) premarket notification submitted by Hospitak, Inc. for the device "DISPOSABLE, HYPERBARIC OXYGEN CHAMBER". The FDA issued a decision of Substantially Equivalent on April 25, 1984. The device falls under product code KPJ (Chamber, Oxygen, Topical, Extremity), a Class II device regulated under 21 CFR 878.5650. Hospitak, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
April 25, 1984
Date Received
February 24, 1984
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Chamber, Oxygen, Topical, Extremity
Device Class
Class II
Regulation Number
878.5650
Review Panel
SU
Submission Type