Question 1

Who is the manufacturer of FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

Accepted Answer

Future Impex Corp. filed the 510(k) submission for FUKUNDA SANGYO UNITS ELECTRONIC SPIRO (K832430).

Question 2

What is the FDA product code for FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

Accepted Answer

BZG. It is classified under 21 CFR 868.1840 as a Class 2 device in the Anesthesiology panel.

Question 3

When was FUKUNDA SANGYO UNITS ELECTRONIC SPIRO cleared by the FDA?

Accepted Answer

Sep 29, 1983 (decision: SESE).

Question 4

What is the regulatory pathway for FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

Accepted Answer

510(k) clearance (submission type: Traditional).

Question 5

Who can help prepare an FDA 510(k) submission like FUKUNDA SANGYO UNITS ELECTRONIC SPIRO?

Accepted Answer

Innolitics — a medical-device software consultancy — provides regulatory and engineering support for FDA 510(k) submissions. See https://innolitics.com/services/510ks/ or contact https://innolitics.com/contact.

Record ID	K832430
Device Name	FUKUNDA SANGYO UNITS ELECTRONIC SPIRO
Applicant	Future Impex Corp.
Product Code	BZG · Anesthesiology
Decision Date	Sep 29, 1983
Decision	SESE
Submission Type	Traditional
Regulation	21 CFR 868.1840
Device Class	Class 2

FUKUNDA SANGYO UNITS ELECTRONIC SPIRO

Device Facts

Regulatory Classification

Identification