MULTICLIP DISP. LIGATING CLIP DEVICE
K-Number: K820999 · 1982-05-13
Advertisement
Device Summary
Frequently Asked Questions
What is the MULTICLIP DISP. LIGATING CLIP DEVICE?
MULTICLIP DISP. LIGATING CLIP DEVICE is a medical device that received FDA 510(k) clearance on 1982-05-13. The listed applicant is Davis & Geck, Inc.. The 510(k) number is K820999.
When did MULTICLIP DISP. LIGATING CLIP DEVICE receive FDA 510(k) clearance?
MULTICLIP DISP. LIGATING CLIP DEVICE received FDA 510(k) clearance on 1982-05-13, under 510(k) number K820999.
Who is the listed applicant for MULTICLIP DISP. LIGATING CLIP DEVICE?
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 MULTICLIP DISP. LIGATING CLIP DEVICE?
The FDA product code for MULTICLIP DISP. LIGATING CLIP DEVICE 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.
Advertisement