510(K) CLEARANCES 67 ▼8RECALLS POSTED 26CLASS I 2PMA DECISIONS 40 ▼14WEEK ENDING / FDA DATA AS OF
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K853980Substantially Equivalent

Erosa Disposable Hypodermic Needle

Rose KG, Washington DC / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K853980 is the FDA 510(k) clearance record for EROSA DISPOSABLE HYPODERMIC NEEDLE, a class I device, cleared for Rose KG on under FDA product code GAA (Needle, Aspiration And Injection, Disposable). FDA records list one 510(k) clearance for Rose KG. As of , FDA records show no recalls naming K853980.

Clearance record

Decision date
Received
(21 days to decision)
Product code
GAA Needle, Aspiration And Injection, Disposable
Regulation
21 CFR 878.4800
Device class
Class I
Review panel
General, Plastic Surgery
Applicant
Rose KG One Farragut Sq. S., Washington DC
Third party review
No

Clearances, product code GAA

Trailing 12 months

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

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