510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K913213Substantially Equivalent

Single Use Lee Electrode

Aspen Laboratories, Inc., Englewood CO / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K913213 is the FDA 510(k) clearance record for SINGLE USE LEE ELECTRODE, a class II device, cleared for Aspen Laboratories, Inc. on under FDA product code HGI (Electrocautery, Gynecologic (And Accessories)). FDA records list 55 510(k) clearances for Aspen Laboratories, Inc., from to . As of , FDA records show no recalls naming K913213.

Clearance record

Decision date
Received
(209 days to decision)
Product code
HGI Electrocautery, Gynecologic (And Accessories)
Regulation
21 CFR 884.4120
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Aspen Laboratories, Inc. P.O. Box 3936, Englewood CO
510(k) summary
Statement
Third party review
No

Clearances, product code HGI

Trailing 12 months

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

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