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

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET

K Number: K884156 · Decision Nov 14, 1988
Classifications
1
FEI Numbers
66
Registration Numbers
66
Same Product Code
63
Applicant Total
23
Review Days
41

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Basic Information

Device Name
HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET
K Number
K884156
Device Class
FDA class 2
Clearance Type
Traditional
Regulation Number
880.5440
Medical Specialty
General Hospital
Decision
Substantially Equivalent
Applicant
Sechrist Industries, Inc.
Date Received
October 4, 1988
Decision Date
November 14, 1988
Product Code
FPK
Advisory Committee
General Hospital
Review Advisory Committee
HO
Third Party
N

Classifications

This FDA 510(k) entry is associated with 1 FDA classification via its product code.

Product Code Device Name
FPK Tubing, Fluid Delivery

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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
K950386 MODEL 3200P/3200PR HYPERBARIC CHAMBER
K930713 THE INFANT FLOW SYSTEM
K914607 SEHRIST VOLUME VENTILATOR, MODEL 2200B
Search all 23 clearances from Sechrist Industries, Inc. →