LEGEND

Table, Powered

HEALTH CARE MFG., INC.

The following data is part of a premarket notification filed by Health Care Mfg., Inc. with the FDA for Legend.

Pre-market Notification Details

• Device ID: K952441
• 510k Number: K952441
• Device Name: LEGEND
• Classification: Table, Powered
• Applicant: HEALTH CARE MFG., INC. 2146 EAST PYTHIAN ST. Springfield, MO 65802
• Contact: Rodney Moulder
• Correspondent: Rodney Moulder; HEALTH CARE MFG., INC. 2146 EAST PYTHIAN ST. Springfield, MO 65802
• Product Code: INQ
• CFR Regulation Number: 890.3760 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1995-05-25
• Decision Date: 1995-06-19