510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K872254Substantially Equivalent

Slt Contact Nd:yag Laser for Intra-Abdom.&genital

Surgical Laser Technologies, Inc., Malvern PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K872254 is the FDA 510(k) clearance record for SLT CONTACT ND:YAG LASER FOR INTRA-ABDOM.&GENITAL, a class II device, cleared for Surgical Laser Technologies, Inc. on under FDA product code HHR (Laser, Surgical, Gynecologic). FDA records list 51 510(k) clearances for Surgical Laser Technologies, Inc., from to . As of , FDA records show no recalls naming K872254.

Clearance record

Decision date
Received
(208 days to decision)
Product code
HHR Laser, Surgical, Gynecologic
Regulation
21 CFR 884.4550
Device class
Class II
Review panel
Obstetrics/Gynecology
Applicant
Surgical Laser Technologies, Inc. One Great Valley Pkwy., Malvern PA
Third party review
No

Clearances, product code HHR

Trailing 12 months

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

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