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FDA 510(k)

PILLING HEMOSTATIC CLIP APPLIER FORCEPS

K-Number: K854916 · 1986-01-24

ApplicantPilling Co.
Decision Date1986-01-24
Product CodeGEN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PILLING HEMOSTATIC CLIP APPLIER FORCEPS 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 K854916. The device is classified under product code GEN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PILLING HEMOSTATIC CLIP APPLIER FORCEPS?

PILLING HEMOSTATIC CLIP APPLIER FORCEPS 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 K854916.

When did PILLING HEMOSTATIC CLIP APPLIER FORCEPS receive FDA 510(k) clearance?

PILLING HEMOSTATIC CLIP APPLIER FORCEPS received FDA 510(k) clearance on 1986-01-24, under 510(k) number K854916.

Who is the listed applicant for PILLING HEMOSTATIC CLIP APPLIER FORCEPS?

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

What is the FDA product code for PILLING HEMOSTATIC CLIP APPLIER FORCEPS?

The FDA product code for PILLING HEMOSTATIC CLIP APPLIER FORCEPS is GEN.

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.

View all 39 devices →

Related Devices (Code: GEN)

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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