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FDA 510(k)

ST-200A W/MAXIMAL VOLUNTARY VENTILLAT-

K-Number: K843700 · 1984-10-24

ApplicantFuture Impex Corp.
Decision Date1984-10-24
Product Code
DecisionSubstantially Equivalent

Device Summary

ST-200A W/MAXIMAL VOLUNTARY VENTILLAT- is the device name listed in this FDA 510(k) record. The listed applicant is Future Impex Corp.. It received FDA 510(k) clearance on 1984-10-24 under 510(k) number K843700. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ST-200A W/MAXIMAL VOLUNTARY VENTILLAT-?

ST-200A W/MAXIMAL VOLUNTARY VENTILLAT- is a medical device that received FDA 510(k) clearance on 1984-10-24. The listed applicant is Future Impex Corp.. The 510(k) number is K843700.

When did ST-200A W/MAXIMAL VOLUNTARY VENTILLAT- receive FDA 510(k) clearance?

ST-200A W/MAXIMAL VOLUNTARY VENTILLAT- received FDA 510(k) clearance on 1984-10-24, under 510(k) number K843700.

Who is the listed applicant for ST-200A W/MAXIMAL VOLUNTARY VENTILLAT-?

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

Related Clinical Trials

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

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Other records listing Future Impex Corp. as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K861487ST-90 SPIRO ANALIZERK854687ERMA HB-METER MODEL 303NK854686TE-25 COAGURO METERK854685DIGITAL-9 KEY LEUCOCYTE COUNTERK854677ERMA PC-604 BLOOD CELL COUNTERK854678ERMA PC-602 PC-603 BLOOD CELL COUNTER

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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.

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