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

SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION

K Number: K850563 · Decision Mar 12, 1985
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
68
Applicant Total
2
Review Days
28

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Basic Information

Device Name
SECHRIST VENTILATOR/NAUTILUS CHAMBER COMBINATION
K Number
K850563
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5470
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Applicant
Nautilus Environmedical Systems, Inc.
Date Received
February 12, 1985
Decision Date
March 12, 1985
Product Code
CBF
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
CBF Chamber, Hyperbaric

Similar 510(k) Clearances

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

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Other Clearances by Nautilus Environmedical Systems, Inc.

K Number Device Name
K832127 NAUTILUS MONOPLACE HYPERBARIC UNIT