AUTOMATIC MULTICLIP DISPOS. LIGATING
K-Number: K843336 · 1984-10-31
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Device Summary
Frequently Asked Questions
What is the AUTOMATIC MULTICLIP DISPOS. LIGATING?
AUTOMATIC MULTICLIP DISPOS. LIGATING is a medical device that received FDA 510(k) clearance on 1984-10-31. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K843336.
When did AUTOMATIC MULTICLIP DISPOS. LIGATING receive FDA 510(k) clearance?
AUTOMATIC MULTICLIP DISPOS. LIGATING received FDA 510(k) clearance on 1984-10-31, under 510(k) number K843336.
Who is the listed applicant for AUTOMATIC MULTICLIP DISPOS. LIGATING?
The FDA 510(k) record lists Davis & Geck, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AUTOMATIC MULTICLIP DISPOS. LIGATING?
The FDA product code for AUTOMATIC MULTICLIP DISPOS. LIGATING is FZP.
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 Davis & Geck, 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: FZP)
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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