SUCTION WOUND DRAINAGE DEVICE— 510(k) K810739

Name: FDA 510(k) clearance K810739
Creator: U.S. Food and Drug Administration
Published: 1981-06-26

Substantially Equivalent

The Urology Group

FDA 510(k) clearance K810739 for SUCTION WOUND DRAINAGE DEVICE, Substantially Equivalent on 1981-06-26. Applicant: The Urology Group. Device class: 2.

Clearance details

Applicant: The Urology Group
Product code: Code KQT
Device class: Class 2
Regulation: 21 CFR 876.4370
Advisory panel: Gastroenterology, Urology
Date received: 1981-03-19
Decision date: 1981-06-26
Decision: Substantially Equivalent
Clearance type: Traditional
Location: Mchenry, IL, US

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Recent devices under product code KQT

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K964111 — LITHOVAC SUCTION/ASPIRATION PROBE1996-12-16
K921088 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K921451 — EVACUATOR, GASTRO-UROLOGY1992-10-28
K910728 — CLEANFLOW SYSTEM1991-04-01
K880099 — VAN-TEC BLADDER EVACUATOR1988-03-02

More clearances from The Urology Group

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K831703 — COVERUPS1984-01-03
K831489 — SURGICAL TUBE HOLDER1983-12-12
K810788 — SURGICAL TUBE HOLDER1981-04-17
K810787 — UROLOGIC TUBE HOLDER1981-03-31
K801629 — COVER-ALL MALE INCONTINENCE DEVICE1980-08-12

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