Morse Hemostatic Catheter Introducer Set

FDA 510(k) K915078 · North American Instrument Corp.

Substantially Equivalent

510(k) numberK915078

Submission

Device name
Morse Hemostatic Catheter Introducer Set
Applicant
North American Instrument Corp.
Glens Falls, NY, US
Received
November 8, 1991
Decision date
June 10, 1992
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
DYB – Introducer, Catheter
Device class
Class II (moderate risk)
Regulation
21 CFR 870.1340
Specialty
Cardiovascular

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Questions and answers

When was Morse Hemostatic Catheter Introducer Set cleared by the FDA?

Morse Hemostatic Catheter Introducer Set (K915078) received a 510(k) decision of Substantially Equivalent on June 10, 1992, 215 days after the submission was received.

What is the product code of K915078?

The FDA product code is DYB – Introducer, Catheter, a Class II (moderate risk) device regulated under 21 CFR 870.1340.