510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K896621Substantially Equivalent

L.t.c. Replacement Gastrostomy Tube

Intl. Medical Marketing, Inc., Ridge NY / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K896621 is the FDA 510(k) clearance record for L.T.C. REPLACEMENT GASTROSTOMY TUBE, a class I device, cleared for Intl. Medical Marketing, Inc. on under FDA product code KCQ (Tube Impression And Matrix). FDA records list 5 510(k) clearances for Intl. Medical Marketing, Inc., from to . As of , FDA records show no recalls naming K896621.

Clearance record

Decision date
Received
(112 days to decision)
Product code
KCQ Tube Impression And Matrix
Regulation
21 CFR 872.6570
Device class
Class I
Review panel
Dental
Applicant
Intl. Medical Marketing, Inc. P.O. Box 578, Ridge NY
Third party review
No

Clearances, product code KCQ

Trailing 12 months

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

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