510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K810920Substantially Equivalent

Ndm Diatemp Infant Electrosurg. Disp. P.

Ndm Corp., Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K810920 is the FDA 510(k) clearance record for NDM DIATEMP INFANT ELECTROSURG. DISP. P., a class II device, cleared for Ndm Corp. on under FDA product code HAM (Apparatus, Electrosurgical). FDA records list 8 510(k) clearances for Ndm Corp., from to . As of , FDA records show no recalls naming K810920.

Clearance record

Decision date
Received
(25 days to decision)
Product code
HAM Apparatus, Electrosurgical
Regulation
21 CFR 878.4400
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Ndm Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code HAM

Trailing 12 months

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

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