ST-460 Spiro Analyzer Spirometer

FDA 510(k) K852308 · Futuremed Div. of Future Impex Corp.

Substantially Equivalent

510(k) numberK852308

Submission

Device name
ST-460 Spiro Analyzer Spirometer
Applicant
Futuremed Div. of Future Impex Corp.
Deerpark, NY, US
Received
May 29, 1985
Decision date
June 24, 1985
Decision
Substantially Equivalent (SESE)
Type
Traditional 510(k)

Official FDA 510(k) record

Device classification

Product code
BZG – Spirometer, Diagnostic
Device class
Class II (moderate risk)
Regulation
21 CFR 868.1840
Specialty
Anesthesiology

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Questions and answers

When was ST-460 Spiro Analyzer Spirometer cleared by the FDA?

ST-460 Spiro Analyzer Spirometer (K852308) received a 510(k) decision of Substantially Equivalent on June 24, 1985, 26 days after the submission was received.

What is the product code of K852308?

The FDA product code is BZG – Spirometer, Diagnostic, a Class II (moderate risk) device regulated under 21 CFR 868.1840.