Morwel Cannula

FDA 510(k) K831520 · Morwel Corp.

Substantially Equivalent

510(k) numberK831520

Submission

Device name
Morwel Cannula
Applicant
Morwel Corp.
Mchenry, IL, US
Received
May 12, 1983
Decision date
June 20, 1983
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

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K962525Ultra-Safe Ultrasonic Aspirator SystemLFL · Traditional 09/19/1996SE
K841160Morwel AspiratorJCX · Traditional 05/31/1984SE
K841159Suction Tips · Traditional 03/19/1984SESP

Questions and answers

When was Morwel Cannula cleared by the FDA?

Morwel Cannula (K831520) received a 510(k) decision of Substantially Equivalent on June 20, 1983, 39 days after the submission was received.