Suction Tips

FDA 510(k) K841159 · Morwel Corp.

Unknown

510(k) numberK841159

Submission

Device name
Suction Tips
Applicant
Morwel Corp.
Mchenry, IL, US
Received
March 19, 1984
Decision date
March 19, 1984
Decision
Unknown (SESP)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

No product code recorded.

More from Morwel Corp.

510(k)DeviceDecision
K962525Ultra-Safe Ultrasonic Aspirator SystemLFL · Traditional 09/19/1996SE
K841160Morwel AspiratorJCX · Traditional 05/31/1984SE
K831520Morwel Cannula · Traditional 06/20/1983SE

Questions and answers

When was Suction Tips cleared by the FDA?

Suction Tips (K841159) received a 510(k) decision of Unknown on March 19, 1984, 0 days after the submission was received.