Stryker Drop Applicator, Kits, Spray Applicator Kit, Tips

FDA 510(k) K950824 · Stryker Corp.

Substantially Equivalent

510(k) numberK950824

Submission

Device name
Stryker Drop Applicator, Kits, Spray Applicator Kit, Tips
Applicant
Stryker Corp.
Kalamazoo, MI, US
Received
February 23, 1995
Decision date
August 25, 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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Questions and answers

When was Stryker Drop Applicator, Kits, Spray Applicator Kit, Tips cleared by the FDA?

Stryker Drop Applicator, Kits, Spray Applicator Kit, Tips (K950824) received a 510(k) decision of Substantially Equivalent on August 25, 1995, 183 days after the submission was received.

What is the product code of K950824?

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