510(k) K950630

WALLACH DIGITAL IMAGING SYSTEM by Wallach Surgical Devices, Inc. — Product Code LMB

K950630 is an FDA 510(k) premarket notification submitted by Wallach Surgical Devices, Inc. for the device "WALLACH DIGITAL IMAGING SYSTEM". The FDA issued a decision of Substantially Equivalent on November 22, 1995. The device falls under product code LMB (Device, Digital Image Storage, Radiological), a Class I device regulated under 21 CFR 892.2010. Wallach Surgical Devices, Inc. has at least 10 other 510(k) clearances on record.

Clearance Details

Decision
SESE (Substantially Equivalent)
Decision Date
November 22, 1995
Date Received
February 13, 1995
Clearance Type
Traditional
Expedited Review
No
Third Party Review
No

Device Classification

Device Name
Device, Digital Image Storage, Radiological
Device Class
Class I
Regulation Number
892.2010
Review Panel
RA
Submission Type

Medical image storage hardware is a device that provides electronic maintenance and access functions for medical images.