510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K761193Substantially Equivalent

Suture Removal Kit

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

K761193 is the FDA 510(k) clearance record for SUTURE REMOVAL KIT, a class I device, cleared for Superior Plastic Products Corp. on under FDA product code KDD (Kit, Surgical Instrument, Disposable). FDA records list 15 510(k) clearances for Superior Plastic Products Corp., from to . As of , FDA records show one recall naming K761193.

Clearance record

Decision date
Received
(37 days to decision)
Product code
KDD Kit, Surgical Instrument, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Superior Plastic Products Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KDD

Trailing 12 months

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

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