GRATICULE

Accelerator, Linear, Medical

MICK RADIO-NUCLEAR INSTRUMENTS, INC.

The following data is part of a premarket notification filed by Mick Radio-nuclear Instruments, Inc. with the FDA for Graticule.

Pre-market Notification Details

• Device ID: K871214
• 510k Number: K871214
• Device Name: GRATICULE
• Classification: Accelerator, Linear, Medical
• Applicant: MICK RADIO-NUCLEAR INSTRUMENTS, INC. P.O. BOX 99 Bronx, NY 10465
• Contact: Felix W Mick
• Correspondent: Felix W Mick; MICK RADIO-NUCLEAR INSTRUMENTS, INC. P.O. BOX 99 Bronx, NY 10465
• Product Code: IYE
• CFR Regulation Number: 892.5050 [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 1987-03-26
• Decision Date: 1987-05-08