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FDA 510(k)

MOBIN-VDDIN VEIN GRAFT HOLDER

K-Number: K854913 · 1986-01-24

ApplicantPilling Co.
Decision Date1986-01-24
Product Code
DecisionSubstantially Equivalent

Device Summary

MOBIN-VDDIN VEIN GRAFT HOLDER is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1986-01-24 under 510(k) number K854913. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MOBIN-VDDIN VEIN GRAFT HOLDER?

MOBIN-VDDIN VEIN GRAFT HOLDER is a medical device that received FDA 510(k) clearance on 1986-01-24. The listed applicant is Pilling Co.. The 510(k) number is K854913.

When did MOBIN-VDDIN VEIN GRAFT HOLDER receive FDA 510(k) clearance?

MOBIN-VDDIN VEIN GRAFT HOLDER received FDA 510(k) clearance on 1986-01-24, under 510(k) number K854913.

Who is the listed applicant for MOBIN-VDDIN VEIN GRAFT HOLDER?

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

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 Pilling Co. 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.

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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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