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FDA 510(k)

MODIFIED WALKMED 400

K-Number: K905783 · 1991-01-11

ApplicantMedfusion, Inc.
Decision Date1991-01-11
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODIFIED WALKMED 400 is the device name listed in this FDA 510(k) record. The listed applicant is Medfusion, Inc.. It received FDA 510(k) clearance on 1991-01-11 under 510(k) number K905783. The device is classified under product code FRN. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODIFIED WALKMED 400?

MODIFIED WALKMED 400 is a medical device that received FDA 510(k) clearance on 1991-01-11. The listed applicant is Medfusion, Inc.. The 510(k) number is K905783.

When did MODIFIED WALKMED 400 receive FDA 510(k) clearance?

MODIFIED WALKMED 400 received FDA 510(k) clearance on 1991-01-11, under 510(k) number K905783.

Who is the listed applicant for MODIFIED WALKMED 400?

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

What is the FDA product code for MODIFIED WALKMED 400?

The FDA product code for MODIFIED WALKMED 400 is FRN.

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Other records listing Medfusion, Inc. 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.

K905029MODEL 2001, MODIFICATIONK901755MODEL 3001 SYRINGE INFUSION PUMPK890862AMBULATORY INFUSION PUMPK890120SYRINGE INFUSION PUMP

Related Devices (Code: FRN)

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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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