Callaly Tampliner
K-Number: K201003 · 2020-12-07
ApplicantCalla Lily Personal Care, Ltd.
Decision Date2020-12-07
Product CodeHEB
Advisory CommitteeOB
DecisionSubstantially Equivalent
Device Summary
Callaly Tampliner is a medical device manufactured by Calla Lily Personal Care, Ltd.. It received FDA 510(k) clearance on 2020-12-07 under approval number K201003. The device is classified under product code HEB. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Callaly Tampliner?
Callaly Tampliner is a medical device that received FDA 510(k) clearance on 2020-12-07. It is manufactured by Calla Lily Personal Care, Ltd.. The 510(k) number is K201003.
When was Callaly Tampliner approved by the FDA?
Callaly Tampliner received FDA 510(k) clearance on 2020-12-07, under approval number K201003.
What company makes Callaly Tampliner?
Callaly Tampliner is manufactured by Calla Lily Personal Care, Ltd..
What is the FDA product code for Callaly Tampliner?
The FDA product code for Callaly Tampliner is HEB.
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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.