510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K231813Substantially Equivalent

Ultrasonic Gastrovideoscope

Sonoscape Medical Corp., Shenzhen, CN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)510(k) summary (opens on fda.gov)

K231813 is the FDA 510(k) clearance record for Ultrasonic Gastrovideoscope, a class II device, cleared for Sonoscape Medical Corp. on under FDA product code ODG (Endoscopic Ultrasound System, Gastroenterology-Urology). FDA's definition for product code ODG reads: "To provide ultrasonic visualization of body cavities that can be accessed by endoscope. For reusable, flexible endoscopes in this product code, validated reprocessing instructions and reprocessing validation data must be included in a...". FDA records list 25 510(k) clearances for Sonoscape Medical Corp., from to . As of , FDA records show no recalls naming K231813.

Clearance record

Decision date
Received
(261 days to decision)
Product code
ODG Endoscopic Ultrasound System, Gastroenterology-Urology
Regulation
21 CFR 876.1500
Device class
Class II
Review panel
Gastroenterology, Urology
Applicant
Sonoscape Medical Corp. Rm. 201 & 202, 12th Bldg., Shenzhen Software Park, Shenzhen, CN
510(k) summary
Summary PDF
Third party review
No

Clearances, product code ODG

Trailing 12 months
2 clearances under product code ODG in the twelve months to October 2026, June 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code ODG, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20261
July 20261
August 20260
September 20260
October 20260