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

MODEL 3200P/3200PR HYPERBARIC CHAMBER

K Number: K950386 · Decision Jun 13, 1995
Classifications
1
FEI Numbers
18
Registration Numbers
18
Same Product Code
68
Applicant Total
23
Review Days
132

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Basic Information

Device Name
MODEL 3200P/3200PR HYPERBARIC CHAMBER
K Number
K950386
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
868.5470
Medical Specialty
Anesthesiology
Decision
Substantially Equivalent
Statement or Summary
Statement
Applicant
Sechrist Industries, Inc.
Date Received
February 1, 1995
Decision Date
June 13, 1995
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

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Other Clearances by Sechrist Industries, Inc.

K Number Device Name
K140559 SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
K100268 SECHRIST MONOPLACE HYPERBARIC OXYGEN CHAMBER
K052713 MODEL 3300E/ER MONOPLACE HYPERBARIC OXYGEN CHAMBER
K023745 SECHRIST AIR/OXYGEN MIXER, MODEL 3500 CP-G
K993167 MILLENNIUM INFANT VENTILATOR
K992503 SECHRIST AIR-OXYGEN MIXER, 3500/3500HL SERIES
K934164 MODEL 2500E/2500ER HYPERBARIC CHAMBER
K930713 THE INFANT FLOW SYSTEM
K914607 SEHRIST VOLUME VENTILATOR, MODEL 2200B
K896269 SECHRIST VOLUME VENTILATOR MODEL 2200B
Search all 23 clearances from Sechrist Industries, Inc. →