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FDA 510(k)

DISPOSABLE DISC FILTER

K-Number: K895419 · 1989-11-24

ApplicantThe Medi-Dose Group
Decision Date1989-11-24
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE DISC FILTER is the device name listed in this FDA 510(k) record. The listed applicant is The Medi-Dose Group. It received FDA 510(k) clearance on 1989-11-24 under 510(k) number K895419. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE DISC FILTER?

DISPOSABLE DISC FILTER is a medical device that received FDA 510(k) clearance on 1989-11-24. The listed applicant is The Medi-Dose Group. The 510(k) number is K895419.

When did DISPOSABLE DISC FILTER receive FDA 510(k) clearance?

DISPOSABLE DISC FILTER received FDA 510(k) clearance on 1989-11-24, under 510(k) number K895419.

Who is the listed applicant for DISPOSABLE DISC FILTER?

The FDA 510(k) record lists The Medi-Dose Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE DISC FILTER?

The FDA product code for DISPOSABLE DISC FILTER is FMF.

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Other records listing The Medi-Dose Group as applicant

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Related Devices (Code: FMF)

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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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