H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG — Rudolf Riester GmbH & Co. KG (510(k) K946043)

Name: H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG — Rudolf Riester GmbH & Co. KG (510(k) K946043)
Creator: DeviceClear

H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG — Rudolf Riester GmbH & Co. KG (510(k) K946043) is one of 9,000 device clearances in the DeviceClear dataset. Key details — Device name: H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG; Applicant: Rudolf Riester GmbH & Co. KG; Clearance track: 510(k).

Device name	H5000, H5000L, H5000L REVERSE MODEL H5000C, H5000CG
Applicant	Rudolf Riester GmbH & Co. KG
Clearance track	510(k)
Submission number	K946043
Decision	Unknown
Decision date	1995-03-08
Date received	1994-12-12
Product code	ERA
Device class	1
Medical specialty	Ear, Nose, Throat
Applicant location	DE
Source	openFDA device

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$1999/mo

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