Allergist Syringes

FDA 510(k) K880894 · Abco Dealers, Inc.

Substantially Equivalent

510(k) numberK880894

Submission

Device name
Allergist Syringes
Applicant
Abco Dealers, Inc.
Milwaukee, WI, US
Received
March 2, 1988
Decision date
March 31, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K905025Digital Thermometer KitsFLL · Traditional 02/07/1991SE
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K872875Stretch Gauze BandagesNAD · Traditional 09/04/1987SE
K872874Microscope Cover GlassesKES · Traditional 08/10/1987SE
K872797Non-Skid Shoe CoversFXP · Traditional 08/04/1987SE
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K862726Disposable Shoe Covers and Nurses CapsFXP · Traditional 08/01/1986SE
K862111Armboards, Reusable and Disposable · Traditional 07/08/1986SE
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Questions and answers

When was Allergist Syringes cleared by the FDA?

Allergist Syringes (K880894) received a 510(k) decision of Substantially Equivalent on March 31, 1988, 29 days after the submission was received.

What is the product code of K880894?

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