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FDA 510(k)

DEMI-WALKER (REGULAR)

K-Number: K772268 · 1977-12-20

ApplicantMed Fusion Systems, Inc.
Decision Date1977-12-20
Product CodeITQ
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

DEMI-WALKER (REGULAR) is the device name listed in this FDA 510(k) record. The listed applicant is Med Fusion Systems, Inc.. It received FDA 510(k) clearance on 1977-12-20 under 510(k) number K772268. The device is classified under product code ITQ. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEMI-WALKER (REGULAR)?

DEMI-WALKER (REGULAR) is a medical device that received FDA 510(k) clearance on 1977-12-20. The listed applicant is Med Fusion Systems, Inc.. The 510(k) number is K772268.

When did DEMI-WALKER (REGULAR) receive FDA 510(k) clearance?

DEMI-WALKER (REGULAR) received FDA 510(k) clearance on 1977-12-20, under 510(k) number K772268.

Who is the listed applicant for DEMI-WALKER (REGULAR)?

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

What is the FDA product code for DEMI-WALKER (REGULAR)?

The FDA product code for DEMI-WALKER (REGULAR) is ITQ.

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Other records listing Med Fusion Systems, Inc. as applicant

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Related Devices (Code: ITQ)

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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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