Suction and Lavage Probe

FDA 510(k) K874614 · Medical Marketing, Inc.

Substantially Equivalent

510(k) numberK874614

Submission

Device name
Suction and Lavage Probe
Applicant
Medical Marketing, Inc.
Fischer, TX, US
Received
November 9, 1987
Decision date
June 23, 1988
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
HET – Laparoscope, Gynecologic (And Accessories)
Device class
Class II (moderate risk)
Regulation
21 CFR 884.1720
Specialty
Obstetrics/Gynecology

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More from 270surgical , Ltd.

510(k)DeviceDecision
K874615Laser Cannister FilterHHR · Traditional 06/23/1988SE
K874612Titanium RodsHET · Traditional 06/23/1988SE
K874611Titanium Backstop with SuctionHET · Traditional 06/23/1988SE

Questions and answers

When was Suction and Lavage Probe cleared by the FDA?

Suction and Lavage Probe (K874614) received a 510(k) decision of Substantially Equivalent on June 23, 1988, 227 days after the submission was received.

What is the product code of K874614?

The FDA product code is HET – Laparoscope, Gynecologic (And Accessories), a Class II (moderate risk) device regulated under 21 CFR 884.1720.