Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

TITANIUM HEMOSTATIC CLIPS

K-Number: K861922 · 1986-06-13

ApplicantPilling Co.
Decision Date1986-06-13
Product CodeFZP
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TITANIUM HEMOSTATIC CLIPS is the device name listed in this FDA 510(k) record. The listed applicant is Pilling Co.. It received FDA 510(k) clearance on 1986-06-13 under 510(k) number K861922. 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 TITANIUM HEMOSTATIC CLIPS?

TITANIUM HEMOSTATIC CLIPS is a medical device that received FDA 510(k) clearance on 1986-06-13. The listed applicant is Pilling Co.. The 510(k) number is K861922.

When did TITANIUM HEMOSTATIC CLIPS receive FDA 510(k) clearance?

TITANIUM HEMOSTATIC CLIPS received FDA 510(k) clearance on 1986-06-13, under 510(k) number K861922.

Who is the listed applicant for TITANIUM HEMOSTATIC CLIPS?

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 TITANIUM HEMOSTATIC CLIPS?

The FDA product code for TITANIUM HEMOSTATIC CLIPS 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 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: 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.

↑