510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K844671Substantially Equivalent

Corning Disposal Sterile Filter System-Nylon

Corning Medical & Scientific, Medfield MA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K844671 is the FDA 510(k) clearance record for CORNING DISPOSAL STERILE FILTER SYSTEM-NYLON, a class I device, cleared for Corning Medical & Scientific on under FDA product code KET (Filters, Cell Collection, Tissue Processing). FDA records list 111 510(k) clearances for Corning Medical & Scientific, from to . As of , FDA records show no recalls naming K844671.

Clearance record

Decision date
Received
(87 days to decision)
Product code
KET Filters, Cell Collection, Tissue Processing
Regulation
21 CFR 864.3010
Device class
Class I
Review panel
Pathology
Applicant
Corning Medical & Scientific Corning Glass Works, Medfield MA
Third party review
No

Clearances, product code KET

Trailing 12 months

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

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