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)

REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS

K-Number: K070930 · 2007-10-18

ApplicantSterilmed, Inc.
Decision Date2007-10-18
Product CodeNLL
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS is the device name listed in this FDA 510(k) record. The listed applicant is Sterilmed, Inc.. It received FDA 510(k) clearance on 2007-10-18 under 510(k) number K070930. The device is classified under product code NLL. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS?

REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS is a medical device that received FDA 510(k) clearance on 2007-10-18. The listed applicant is Sterilmed, Inc.. The 510(k) number is K070930.

When did REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS receive FDA 510(k) clearance?

REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS received FDA 510(k) clearance on 2007-10-18, under 510(k) number K070930.

Who is the listed applicant for REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS?

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

What is the FDA product code for REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS?

The FDA product code for REPROCESSED AUTOSUTURE GIA ENDOSCOPIC STAPLERS is NLL.

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

Other records listing Sterilmed, Inc. 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.

K254149Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510825); Reprocessed AcuNav CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657484); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on Siemens System (R11510826); Reprocessed SOUNDSTAR CRYSTAL™ Ultrasound Catheter 9F x 90 CM, For Use on GE System (R11657485)K240826Reprocessed DECANAV™ Electrophysiology Catheter; Reprocessed WEBSTER® Duo-Decapolar Electrophysiology CatheterK190478Reprocessed ViewFlex™ Xtra ICE CatheterK190610Reprocessed HARMONIC FOCUS Shears + Adaptive Tissue TechnologyK182272Reprocessed HARMONIC ACE+ 7 Shears with Advanced HemostasisK161700SoundStar eco 8F 3D Diagnostic eco Ultrasound Catheters, SoundStar eco 8F G 3D Diagnostic eco Ultrasound Catheters

View all 60 devices →

Related Devices (Code: NLL)

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.

K070859REPROCESSED ETHICON ETS ENDOSCOPIC LINEAR CUTTERSSterilmed, Inc.K033578REPROCESSED RELOADABLE CUTTERS, STAPLERS, AND APPLIERSClearmedical, 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.

↑