510(k) K884156

HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET by Sechrist Industries, Inc. — Product Code FPK

K884156 is an FDA 510(k) premarket notification submitted by Sechrist Industries, Inc. for the device "HYPERBARIC INTRAVENOUS INFUSION EXTENSION SET". The FDA issued a decision of Substantially Equivalent on November 14, 1988. The device falls under product code FPK (Tubing, Fluid Delivery), a Class II device regulated under 21 CFR 880.5440. Sechrist Industries, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 14, 1988
Date Received
October 4, 1988
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Tubing, Fluid Delivery
Device Class
Class II
Regulation Number
880.5440
Review Panel
HO
Submission Type