510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K791345Substantially Equivalent

Medicine Cup

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

K791345 is the FDA 510(k) clearance record for MEDICINE CUP, a class I device, cleared for General Clinical Plastics Corp. on under FDA product code KYW (Container, Liquid Medication, Graduated). FDA records list 4 510(k) clearances for General Clinical Plastics Corp., from to . As of , FDA records show no recalls naming K791345.

Clearance record

Decision date
Received
(22 days to decision)
Product code
KYW Container, Liquid Medication, Graduated
Regulation
21 CFR 880.6430
Device class
Class I
Review panel
General Hospital
Applicant
General Clinical Plastics Corp. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code KYW

Trailing 12 months

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

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