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FDA 510(k)

V. MUELLER VITAL CLIP-HEMOSTATIC CLIP

K-Number: K861471 · 1986-06-06

Decision Date1986-06-06
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

V. MUELLER VITAL CLIP-HEMOSTATIC CLIP is the device name listed in this FDA 510(k) record. The listed applicant is American V. Mueller. It received FDA 510(k) clearance on 1986-06-06 under 510(k) number K861471. 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 V. MUELLER VITAL CLIP-HEMOSTATIC CLIP?

V. MUELLER VITAL CLIP-HEMOSTATIC CLIP is a medical device that received FDA 510(k) clearance on 1986-06-06. The listed applicant is American V. Mueller. The 510(k) number is K861471.

When did V. MUELLER VITAL CLIP-HEMOSTATIC CLIP receive FDA 510(k) clearance?

V. MUELLER VITAL CLIP-HEMOSTATIC CLIP received FDA 510(k) clearance on 1986-06-06, under 510(k) number K861471.

Who is the listed applicant for V. MUELLER VITAL CLIP-HEMOSTATIC CLIP?

The FDA 510(k) record lists American V. Mueller as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for V. MUELLER VITAL CLIP-HEMOSTATIC CLIP?

The FDA product code for V. MUELLER VITAL CLIP-HEMOSTATIC CLIP 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 American V. Mueller 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 31 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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