510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K833502Substantially Equivalent

Radovan Subcutaneous Tissue Expander

American Heyer Schulte, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K833502 is the FDA 510(k) clearance record for RADOVAN SUBCUTANEOUS TISSUE EXPANDER, cleared for American Heyer Schulte on under FDA product code LCJ (Tissue Expander And Accessories). FDA records list 13 510(k) clearances for American Heyer Schulte, from to . As of , FDA records show no recalls naming K833502.

Clearance record

Decision date
Received
(121 days to decision)
Product code
LCJ Tissue Expander And Accessories
Device class
Unclassified
Review panel
Unknown
Applicant
American Heyer Schulte 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code LCJ

Trailing 12 months
1 clearance under product code LCJ in the twelve months to October 2026, January 2026 the highest month at 1.
Show the numbers
Monthly 510(k) clearances under FDA product code LCJ, trailing twelve months
MonthClearances
November 20250
December 20250
January 20261
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260