FDA 510(k)

SPIROVISION

K-Number: K864885 · 1987-01-15

ApplicantFuturemed Div. of Future Impex Corp.

Decision Date1987-01-15

Product CodeBZM

Advisory CommitteeAN

DecisionSubstantially Equivalent

Device Summary

SPIROVISION is the device name listed in this FDA 510(k) record. The listed applicant is Futuremed Div. of Future Impex Corp.. It received FDA 510(k) clearance on 1987-01-15 under 510(k) number K864885. The device is classified under product code BZM. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPIROVISION?

SPIROVISION is a medical device that received FDA 510(k) clearance on 1987-01-15. The listed applicant is Futuremed Div. of Future Impex Corp.. The 510(k) number is K864885.

When did SPIROVISION receive FDA 510(k) clearance?

SPIROVISION received FDA 510(k) clearance on 1987-01-15, under 510(k) number K864885.

Who is the listed applicant for SPIROVISION?

The FDA 510(k) record lists Futuremed Div. of Future Impex Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SPIROVISION?

The FDA product code for SPIROVISION is BZM.

Related Clinical Trials

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Other records listing Futuremed Div. of Future Impex Corp. as applicant

K933511UPGRADED SPIROMETER ST-90 K933220SELECTOR SL 01 K933222AUDIOMETER DA 323 K903017MEGA-TENS DUAL CHANNEL T.E.N.S.K901308SPIRO ANALYZER MODEL ST 250 K884972TRANSCOUTANEOUS ELECTRO-NEURO STIMULATOR

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Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.