WANDER CARE
K-Number: K925529 · 1993-06-16
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Device Summary
Frequently Asked Questions
What is the WANDER CARE?
WANDER CARE is a medical device that received FDA 510(k) clearance on 1993-06-16. The listed applicant is Care Electronics, Inc.. The 510(k) number is K925529.
When did WANDER CARE receive FDA 510(k) clearance?
WANDER CARE received FDA 510(k) clearance on 1993-06-16, under 510(k) number K925529.
Who is the listed applicant for WANDER CARE?
The FDA 510(k) record lists Care Electronics, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WANDER CARE?
The FDA product code for WANDER CARE is KMI.
Related Clinical Trials
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.
Other records listing Care Electronics, 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.
Related Devices (Code: KMI)
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.
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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