510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K912700Substantially Equivalent

Flocare Dry Cas Sampling Port Models

Flocare Medical, Wayne PA / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K912700 is the FDA 510(k) clearance record for FLOCARE DRY CAS SAMPLING PORT MODELS, a class I device, cleared for Flocare Medical on under FDA product code BYD (Condenser, Heat And Moisture (Artificial Nose)). FDA records list 5 510(k) clearances for Flocare Medical, from to . As of , FDA records show no recalls naming K912700.

Clearance record

Decision date
Received
(84 days to decision)
Product code
BYD Condenser, Heat And Moisture (Artificial Nose)
Regulation
21 CFR 868.5375
Device class
Class I
Review panel
Anesthesiology
Applicant
Flocare Medical 992 Eagle School Rd., Wayne PA
510(k) summary
Statement
Third party review
No

Clearances, product code BYD

Trailing 12 months

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

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