510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K905480Substantially Equivalent

Spiroscope

Grandcor Medical Systems, Dayton OH / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K905480 is the FDA 510(k) clearance record for SPIROSCOPE, a class II device, cleared for Grandcor Medical Systems on under FDA product code BZC (Calculator, Pulmonary Function Data). FDA records list 8 510(k) clearances for Grandcor Medical Systems, from to . As of , FDA records show no recalls naming K905480.

Clearance record

Decision date
Received
(151 days to decision)
Product code
BZC Calculator, Pulmonary Function Data
Regulation
21 CFR 868.1880
Device class
Class II
Review panel
Anesthesiology
Applicant
Grandcor Medical Systems 405 Grand Ave., Dayton OH
Third party review
No

Clearances, product code BZC

Trailing 12 months

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

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