Macro Suction Tube Model No 10061

FDA 510(k) K950754 · Dlp, Inc.

Substantially Equivalent

510(k) numberK950754

Submission

Device name
Macro Suction Tube Model No 10061
Applicant
Dlp, Inc.
Grand Rapids, MI, US
Received
February 17, 1995
Decision date
April 25, 1995
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GCY – Apparatus, Suction, Single Patient Use, Portable, Nonpowered
Device class
Class I (low risk)
Regulation
21 CFR 878.4680
Specialty
General, Plastic Surgery

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K960099Penrose Drain Models 6001 - 6007GCY · Traditional Sil-Med Corp.03/11/1996SE
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K933319Birtcher GS-9480 Integrated 3-CHIP Camera/Xenon Light Source Visualization SystemGCY · Traditional Birtcher Medical Systems, Inc.10/27/1993SE
K933306Imc 5.0MM Irrigation/Aspiration Probe W/HolesGCY · Traditional Inman Medical Corp.10/05/1993SE
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K933170Inman Poole Tip Suction Probe W/Tubing KitGCY · Traditional Inman Medical Corp.09/16/1993SE

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Questions and answers

When was Macro Suction Tube Model No 10061 cleared by the FDA?

Macro Suction Tube Model No 10061 (K950754) received a 510(k) decision of Substantially Equivalent on April 25, 1995, 67 days after the submission was received.

What is the product code of K950754?

The FDA product code is GCY – Apparatus, Suction, Single Patient Use, Portable, Nonpowered, a Class I (low risk) device regulated under 21 CFR 878.4680.