510(K) CLEARANCES 75 ▼9RECALLS POSTED 26 ▼13CLASS I 2 ▼4PMA DECISIONS 54 ▲7WEEK ENDING / FDA DATA AS OF
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K880207Substantially Equivalent for Some Indications

Expandover Elastic Bandage

Expandover C/O Hale and Dorr, Boston MA / Traditional, Substantially Equivalent for Some Indications
FDA source (opens on fda.gov)

K880207 is the FDA 510(k) clearance record for EXPANDOVER ELASTIC BANDAGE, a class I device, cleared for Expandover C/O Hale and Dorr on under FDA product code KGX (Tape And Bandage, Adhesive). FDA records list one 510(k) clearance for Expandover C/O Hale and Dorr. As of , FDA records show no recalls naming K880207.

Clearance record

Decision date
Received
(97 days to decision)
Product code
KGX Tape And Bandage, Adhesive
Regulation
21 CFR 880.5240
Device class
Class I
Review panel
General Hospital
Applicant
Expandover C/O Hale and Dorr 60 State St., Boston MA
Third party review
No

Clearances, product code KGX

Trailing 12 months

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

FDA records show no clearances under product code KGX in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code KGX, 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