P-S Suction Reservoir

FDA 510(k) K801443 · Pudenz-Schulte Medical Research Corp.

Substantially Equivalent

510(k) numberK801443

Submission

Device name
P-S Suction Reservoir
Applicant
Pudenz-Schulte Medical Research Corp.
Mchenry, IL, US
Received
June 20, 1980
Decision date
July 14, 1980
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

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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K963839Cordis Suction Reservoir - Model Number: 910-500GCY · Traditional Cordis Corp.12/12/1996SE
K960099Penrose Drain Models 6001 - 6007GCY · Traditional Sil-Med Corp.03/11/1996SE
K950754Macro Suction Tube Model No 10061GCY · Traditional Dlp, Inc.04/25/1995SE
K936223Pressure Irrigating SystemGCY · Traditional Level 1 Technologies, Inc.05/12/1994SE
K930615Autovac Closed Wound Suction SystemGCY · Traditional Boehringer Laboratories02/22/1994SE
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
K933305Imc 5.0MM Irrigation/Aspiration ProbeGCY · Traditional Inman Medical Corp.10/05/1993SE

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Questions and answers

When was P-S Suction Reservoir cleared by the FDA?

P-S Suction Reservoir (K801443) received a 510(k) decision of Substantially Equivalent on July 14, 1980, 24 days after the submission was received.

What is the product code of K801443?

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.