WAHL FRESH FACE
K-Number: K944909 · 1995-05-08
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Device Summary
Frequently Asked Questions
What is the WAHL FRESH FACE?
WAHL FRESH FACE is a medical device that received FDA 510(k) clearance on 1995-05-08. The listed applicant is Wahl Clipper Corp.. The 510(k) number is K944909.
When did WAHL FRESH FACE receive FDA 510(k) clearance?
WAHL FRESH FACE received FDA 510(k) clearance on 1995-05-08, under 510(k) number K944909.
Who is the listed applicant for WAHL FRESH FACE?
The FDA 510(k) record lists Wahl Clipper Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for WAHL FRESH FACE?
The FDA product code for WAHL FRESH FACE is IRO.
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 Wahl Clipper Corp. 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: IRO)
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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