510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K932278Substantially Equivalent

Pfm Professional 7000 Spirometer

Advanced Medical Systems, Inc., Minneapolis MN / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K932278 is the FDA 510(k) clearance record for PFM PROFESSIONAL 7000 SPIROMETER, a class II device, cleared for Advanced Medical Systems, Inc. on under FDA product code BTY (Calculator, Predicted Values, Pulmonary Function). FDA records list 10 510(k) clearances for Advanced Medical Systems, Inc., from to . As of , FDA records show no recalls naming K932278.

Clearance record

Decision date
Received
(219 days to decision)
Product code
BTY Calculator, Predicted Values, Pulmonary Function
Regulation
21 CFR 868.1890
Device class
Class II
Review panel
Anesthesiology
Applicant
Advanced Medical Systems, Inc. C/O C.G. Bundy Associates, Minneapolis MN
510(k) summary
Statement
Third party review
No

Clearances, product code BTY

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