K831936Substantially Equivalent

Pre-Rolled Tubular Stockinette

Name: K831936 Pre-Rolled Tubular Stockinette
Creator: Ormed Mfg., Inc.
Published: 1983-12-30
License: https://open.fda.gov/license/

Ormed Mfg., Inc., Mchenry IL / Traditional, Substantially Equivalent

FDA source

K831936 is the FDA 510(k) clearance record for PRE-ROLLED TUBULAR STOCKINETTE, cleared for Ormed Mfg., Inc. on 1983-12-30. FDA records list 23 510(k) clearances for Ormed Mfg., Inc., from 1983-09-12 to 1994-01-31. As of 2026-09-10, FDA records show no recalls naming K831936.

Clearance record

Decision date: 1983-12-30
Received: 1983-06-15 (198 days to decision)
Review panel: Unknown
Applicant: Ormed Mfg., Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review: No