CRYOSTAT

Device, Thermal, Hemorrhoids

LIL DRUG STORE PRODUCTS, INC.

The following data is part of a premarket notification filed by Lil Drug Store Products, Inc. with the FDA for Cryostat.

Pre-market Notification Details

• Device ID: K072414
• 510k Number: K072414
• Device Name: CRYOSTAT
• Classification: Device, Thermal, Hemorrhoids
• Applicant: LIL DRUG STORE PRODUCTS, INC. 1201 CONTINENTAL PL. N.E. Cedar Rapids, IA 52402
• Contact: Patricia L Miller
• Correspondent: Patricia L Miller; LIL DRUG STORE PRODUCTS, INC. 1201 CONTINENTAL PL. N.E. Cedar Rapids, IA 52402
• Product Code: LKX
• CFR Regulation Number: 510(k) Premarket Notification [🔎]
• Decision: Substantially Equivalent (SESE)
• Type: Traditional
• 3rd Party Reviewed: No
• Combination Product: No
• Date Received: 2007-08-28
• Decision Date: 2008-04-07
• Summary: summary