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FDA 510(k)

COMBI-CAP

K-Number: K892428 · 1989-07-14

ApplicantThe Medi-Dose Group
Decision Date1989-07-14
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COMBI-CAP 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 1989-07-14 under 510(k) number K892428. 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 COMBI-CAP?

COMBI-CAP is a medical device that received FDA 510(k) clearance on 1989-07-14. The listed applicant is The Medi-Dose Group. The 510(k) number is K892428.

When did COMBI-CAP receive FDA 510(k) clearance?

COMBI-CAP received FDA 510(k) clearance on 1989-07-14, under 510(k) number K892428.

Who is the listed applicant for COMBI-CAP?

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 COMBI-CAP?

The FDA product code for COMBI-CAP 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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