510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K873038Substantially Equivalent

Techton Protective Pad

Techton, Inc., Albuquerque NM / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K873038 is the FDA 510(k) clearance record for TECHTON PROTECTIVE PAD, a class I device, cleared for Techton, Inc. on under FDA product code IWQ (Curtain, Protective, Radiographic). FDA records list one 510(k) clearance for Techton, Inc. As of , FDA records show no recalls naming K873038.

Clearance record

Decision date
Received
(608 days to decision)
Product code
IWQ Curtain, Protective, Radiographic
Regulation
21 CFR 892.6500
Device class
Class I
Review panel
Radiology
Applicant
Techton, Inc. 3116 Camino Real Ct. NE, Albuquerque NM
Third party review
No

Clearances, product code IWQ

Trailing 12 months

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

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