Surgical Technologies, Inc. Syringe

FDA 510(k) K951918 · Surgical Technologies, Inc.

Substantially Equivalent

510(k) numberK951918

Submission

Device name
Surgical Technologies, Inc. Syringe
Applicant
Surgical Technologies, Inc.
Salt Lake City, UT, US
Received
April 24, 1995
Decision date
July 20, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) summary available from FDA

Official FDA 510(k) record

Device classification

Product code
FMF – Syringe, Piston
Device class
Class II (moderate risk)
Regulation
21 CFR 880.5860
Specialty
General Hospital

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More from Instylla, Inc.

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K950683Arthrogram TrayJAA · Traditional 05/06/1995SE
K946135Infinitech Aspirating Laser ProbeHQE · Traditional 04/18/1995SE
K946181Infinitech Soft Tip Flute NeedleHQE · Traditional 03/14/1995SE
K942030Biopsy ScissorsOCZ · Traditional 06/27/1994SE
K942482Pressure Monitoring ExtensionDQO · Traditional 06/14/1994SE
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Questions and answers

When was Surgical Technologies, Inc. Syringe cleared by the FDA?

Surgical Technologies, Inc. Syringe (K951918) received a 510(k) decision of Substantially Equivalent on July 20, 1995, 87 days after the submission was received.

What is the product code of K951918?

The FDA product code is FMF – Syringe, Piston, a Class II (moderate risk) device regulated under 21 CFR 880.5860.