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FDA 510(k)

HOSPITEC MEDI-BUTLER

K-Number: K954500 · 1996-01-18

ApplicantHospitec, Inc.
Decision Date1996-01-18
Product CodeFMI
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

HOSPITEC MEDI-BUTLER is the device name listed in this FDA 510(k) record. The listed applicant is Hospitec, Inc.. It received FDA 510(k) clearance on 1996-01-18 under 510(k) number K954500. The device is classified under product code FMI. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the HOSPITEC MEDI-BUTLER?

HOSPITEC MEDI-BUTLER is a medical device that received FDA 510(k) clearance on 1996-01-18. The listed applicant is Hospitec, Inc.. The 510(k) number is K954500.

When did HOSPITEC MEDI-BUTLER receive FDA 510(k) clearance?

HOSPITEC MEDI-BUTLER received FDA 510(k) clearance on 1996-01-18, under 510(k) number K954500.

Who is the listed applicant for HOSPITEC MEDI-BUTLER?

The FDA 510(k) record lists Hospitec, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for HOSPITEC MEDI-BUTLER?

The FDA product code for HOSPITEC MEDI-BUTLER is FMI.

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Related Devices (Code: FMI)

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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Official Source

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

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