510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K760817Substantially Equivalent

Orthopedic Tubular Stockinette

Parke-Davis Co., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K760817 is the FDA 510(k) clearance record for ORTHOPEDIC TUBULAR STOCKINETTE, a class I device, cleared for Parke-Davis Co. on under FDA product code ILG (Stocking, Elastic). FDA records list 47 510(k) clearances for Parke-Davis Co., from to . As of , FDA records show no recalls naming K760817.

Clearance record

Decision date
Received
(8 days to decision)
Product code
ILG Stocking, Elastic
Regulation
21 CFR 890.3475
Device class
Class I
Review panel
Physical Medicine
Applicant
Parke-Davis Co. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code ILG

Trailing 12 months

FDA records hold no clearances under product code ILG in the trailing twelve months.

FDA records show no clearances under product code ILG in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code ILG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260