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)

SURGEONS CHOICE STAPLE, REMOVE/IMPLANT

K-Number: K802783 · 1980-12-16

ApplicantHospital Products Intl.
Decision Date1980-12-16
Product CodeGBN
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SURGEONS CHOICE STAPLE, REMOVE/IMPLANT is the device name listed in this FDA 510(k) record. The listed applicant is Hospital Products Intl.. It received FDA 510(k) clearance on 1980-12-16 under 510(k) number K802783. The device is classified under product code GBN. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SURGEONS CHOICE STAPLE, REMOVE/IMPLANT?

SURGEONS CHOICE STAPLE, REMOVE/IMPLANT is a medical device that received FDA 510(k) clearance on 1980-12-16. The listed applicant is Hospital Products Intl.. The 510(k) number is K802783.

When did SURGEONS CHOICE STAPLE, REMOVE/IMPLANT receive FDA 510(k) clearance?

SURGEONS CHOICE STAPLE, REMOVE/IMPLANT received FDA 510(k) clearance on 1980-12-16, under 510(k) number K802783.

Who is the listed applicant for SURGEONS CHOICE STAPLE, REMOVE/IMPLANT?

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

What is the FDA product code for SURGEONS CHOICE STAPLE, REMOVE/IMPLANT?

The FDA product code for SURGEONS CHOICE STAPLE, REMOVE/IMPLANT is GBN.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Related Devices (Code: GBN)

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.

K931607MEDDRAINSArmm, Inc.

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.

↑