Hyperbaric Intravenous Infusion Extension Set

FDA 510(k) K884156 · Sechrist Industries, Inc.

Substantially Equivalent

510(k) numberK884156

Submission

Device name
Hyperbaric Intravenous Infusion Extension Set
Applicant
Sechrist Industries, Inc.
Anaheim, CA, US
Received
October 4, 1988
Decision date
November 14, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
FPK – Tubing, Fluid Delivery
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5440
Specialty
General Hospital

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K950386Model 3200P/3200PR Hyperbaric ChamberCBF · Traditional 06/13/1995SE
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Questions and answers

When was Hyperbaric Intravenous Infusion Extension Set cleared by the FDA?

Hyperbaric Intravenous Infusion Extension Set (K884156) received a 510(k) decision of Substantially Equivalent on November 14, 1988, 41 days after the submission was received.

What is the product code of K884156?

The FDA product code is FPK – Tubing, Fluid Delivery, a Class II (moderate risk) device regulated under 21 CFR 880.5440.