Collagen P.I.N. (Percutaneous Induction Needling)
K-Number: K222199 · 2022-10-21
ApplicantInduction Therapies, LLC
Decision Date2022-10-21
Product CodeQAI
Advisory CommitteeSU
DecisionSubstantially Equivalent
Device Summary
Collagen P.I.N. (Percutaneous Induction Needling) is a medical device manufactured by Induction Therapies, LLC. It received FDA 510(k) clearance on 2022-10-21 under approval number K222199. The device is classified under product code QAI. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.
Frequently Asked Questions
What is the Collagen P.I.N. (Percutaneous Induction Needling)?
Collagen P.I.N. (Percutaneous Induction Needling) is a medical device that received FDA 510(k) clearance on 2022-10-21. It is manufactured by Induction Therapies, LLC. The 510(k) number is K222199.
When was Collagen P.I.N. (Percutaneous Induction Needling) approved by the FDA?
Collagen P.I.N. (Percutaneous Induction Needling) received FDA 510(k) clearance on 2022-10-21, under approval number K222199.
What company makes Collagen P.I.N. (Percutaneous Induction Needling)?
Collagen P.I.N. (Percutaneous Induction Needling) is manufactured by Induction Therapies, LLC.
What is the FDA product code for Collagen P.I.N. (Percutaneous Induction Needling)?
The FDA product code for Collagen P.I.N. (Percutaneous Induction Needling) is QAI.
Related Clinical Trials
Related Devices (Code: QAI)
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.