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FDA 510(k)

WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS

K-Number: K991275 · 1999-07-01

ApplicantMckinley, Inc.
Decision Date1999-07-01
Product CodeFRN
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS is the device name listed in this FDA 510(k) record. The listed applicant is Mckinley, Inc.. It received FDA 510(k) clearance on 1999-07-01 under 510(k) number K991275. 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 WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS?

WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS is a medical device that received FDA 510(k) clearance on 1999-07-01. The listed applicant is Mckinley, Inc.. The 510(k) number is K991275.

When did WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS receive FDA 510(k) clearance?

WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS received FDA 510(k) clearance on 1999-07-01, under 510(k) number K991275.

Who is the listed applicant for WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS?

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

What is the FDA product code for WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS?

The FDA product code for WALKMED 300, WALKMED 350, WALKMED IC, WALKMED PCA, WALKMED PLUS is FRN.

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Other records listing Mckinley, 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.

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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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