510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
Medical Device
ManufacturingTHE TRADE PAPER OF THE FACTORY FLOOR
SUBSCRIBE / SIGN IN
K970893Substantially Equivalent

Ultrasound Transducer Drape

Protek Medical Products, Inc., Iowa City IA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K970893 is the FDA 510(k) clearance record for ULTRASOUND TRANSDUCER DRAPE, a class II device, cleared for Protek Medical Products, Inc. on under FDA product code FYA (Gown, Surgical). FDA records list 9 510(k) clearances for Protek Medical Products, Inc., from to . As of , FDA records show no recalls naming K970893.

Clearance record

Decision date
Received
(223 days to decision)
Product code
FYA Gown, Surgical
Regulation
21 CFR 878.4040
Device class
Class II
Review panel
General, Plastic Surgery
Applicant
Protek Medical Products, Inc. 221 E. Market St. Suite 291, Iowa City IA
510(k) summary
Summary
Third party review
No

Clearances, product code FYA

Trailing 12 months
10 clearances under product code FYA in the twelve months to October 2026, February 2026 the highest month at 2.
Show the numbers
Monthly 510(k) clearances under FDA product code FYA, trailing twelve months
MonthClearances
November 20250
December 20251
January 20260
February 20262
March 20260
April 20262
May 20261
June 20261
July 20261
August 20262
September 20260
October 20260