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FDA 510(k)

MULTICLIP DISP. LIGATING CLIP DEVICE

K-Number: K820999 · 1982-05-13

Decision Date1982-05-13
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MULTICLIP DISP. LIGATING CLIP DEVICE is the device name listed in this FDA 510(k) record. The listed applicant is Davis & Geck, Inc.. It received FDA 510(k) clearance on 1982-05-13 under 510(k) number K820999. The device is classified under product code FZP. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 45 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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