Panpac Flexi Shelf Pessary
K-Number: K173351 · 2018-10-31
ApplicantPanpac Medical Corporation
Decision Date2018-10-31
Product CodeHHW
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Panpac Flexi Shelf Pessary is a medical device manufactured by Panpac Medical Corporation. It received FDA 510(k) clearance on 2018-10-31 under approval number K173351. The device is classified under product code HHW. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Panpac Flexi Shelf Pessary?
Panpac Flexi Shelf Pessary is a medical device that received FDA 510(k) clearance on 2018-10-31. It is manufactured by Panpac Medical Corporation. The 510(k) number is K173351.
When was Panpac Flexi Shelf Pessary approved by the FDA?
Panpac Flexi Shelf Pessary received FDA 510(k) clearance on 2018-10-31, under approval number K173351.
What company makes Panpac Flexi Shelf Pessary?
Panpac Flexi Shelf Pessary is manufactured by Panpac Medical Corporation.
What is the FDA product code for Panpac Flexi Shelf Pessary?
The FDA product code for Panpac Flexi Shelf Pessary is HHW.
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Official Source
View on FDA Database →Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.