FDA 510(k) Application Details - K240457

Device Classification Name	Unit, Cryosurgical, Accessories   More FDA Info for this Device
510(K) Number	K240457
Device Name	Unit, Cryosurgical, Accessories
Applicant	PENTAX of America, Inc. 3 Paragon Drive Montvale, NJ 07645 US Other 510(k) Applications for this Company
Contact	Gurvinder Singh Nanda Other 510(k) Applications for this Contact
Regulation Number	878.4350   More FDA Info for this Regulation Number
Classification Product Code	GEH Other 510(k) Applications for this Device   More FDA Info for this Product Code
Date Received	02/16/2024
Decision Date	07/24/2024
Decision	SESE - SUBST EQUIV
Classification Advisory Committee	SU - General & Plastic Surgery
Review Advisory Committee	SU - General & Plastic Surgery
Statement / Summary / Purged Status	Summary
Type	Traditional
Reviewed By Third Party	N
Expedited Review