Kendall Wound Drainage Systems-Trocars

FDA 510(k) K925805 · Kendall Healthcare Products Co. Div.Of Tyco Health

Substantially Equivalent

510(k) numberK925805

Submission

Device name
Kendall Wound Drainage Systems-Trocars
Applicant
Kendall Healthcare Products Co. Div.Of Tyco Health
Mansfield, MA, US
Received
November 16, 1992
Decision date
February 26, 1993
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)
Summary
510(k) statement available from FDA

Official FDA 510(k) record

Device classification

Product code
GBX – Catheter, Irrigation
Device class
Class I (low risk)
Regulation
21 CFR 878.4200
Specialty
General, Plastic Surgery

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K974233Lysonix Irrigation SystemGBX · Traditional Lysonix, Inc.02/03/1998SE
K973703Jackson-Pratt Hemaduct Wound Drain, Jackson-Pratt Gold Hemaduct Wound DrainGBX · Traditional Allegiance Healthcare Corp.12/04/1997SE
K972635Ultracell Suction SpongeGBX · Traditional Ultracell Medical Technologies, Inc.10/01/1997SE
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More from Axiom Medical, Inc.

510(k)DeviceDecision
K973763Kendall Curity Iodoform Packing StripEFQ · Traditional 12/31/1997SE
K973511Kendall Curity Petrolatum GauzeFRO · Traditional 12/16/1997SN
K973507Kendall Xeroform Petrolatum Dressing (6311,6312,6313,6314,6315,6316,6317)FRO · Traditional 12/15/1997SN
K973619Kendall Curity Non-Adhering DressingKMF · Traditional 12/10/1997SN
K973509Kendall Curasorb ZN + MG Alginate Wound DressingKMF · Traditional 12/04/1997SN
K973546Kendall Fast-Cath Pre Lubricated Urethral CatheterEZD · Traditional 11/07/1997SE
K970266Kendall Hydrophilic Powder Wound DressingKGN · Traditional 04/23/1997SN
K963446Kendall Dual Lumen CatheterMPB · Traditional 03/18/1997SE
K964899Kendall Curity Ureteral CatheterEYB · Traditional 02/07/1997SE
K964519Curity Thoracentesis TrayGCX · Traditional 12/20/1996SE

Questions and answers

When was Kendall Wound Drainage Systems-Trocars cleared by the FDA?

Kendall Wound Drainage Systems-Trocars (K925805) received a 510(k) decision of Substantially Equivalent on February 26, 1993, 102 days after the submission was received.

What is the product code of K925805?

The FDA product code is GBX – Catheter, Irrigation, a Class I (low risk) device regulated under 21 CFR 878.4200.