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)

ANCHOR BRAND SURGICAL NEEDLES

K-Number: K831648 · 1983-08-16

ApplicantAnchor Products Co.
Decision Date1983-08-16
Product CodeGAB
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

ANCHOR BRAND SURGICAL NEEDLES is the device name listed in this FDA 510(k) record. The listed applicant is Anchor Products Co.. It received FDA 510(k) clearance on 1983-08-16 under 510(k) number K831648. The device is classified under product code GAB. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ANCHOR BRAND SURGICAL NEEDLES?

ANCHOR BRAND SURGICAL NEEDLES is a medical device that received FDA 510(k) clearance on 1983-08-16. The listed applicant is Anchor Products Co.. The 510(k) number is K831648.

When did ANCHOR BRAND SURGICAL NEEDLES receive FDA 510(k) clearance?

ANCHOR BRAND SURGICAL NEEDLES received FDA 510(k) clearance on 1983-08-16, under 510(k) number K831648.

Who is the listed applicant for ANCHOR BRAND SURGICAL NEEDLES?

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

What is the FDA product code for ANCHOR BRAND SURGICAL NEEDLES?

The FDA product code for ANCHOR BRAND SURGICAL NEEDLES is GAB.

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 Anchor Products 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.

K091930ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEM, MODEL TRS100SBK061555ANCHOR LAPARSCOPIC TISSUE RETIEVAL SYSTEMK982073ANCHOR LAPAROSCOPIC TISSUE RETRIEVAL SYSTEMK884862ANCHOR DOUBLE-EDGE MYRINGOTOMY BLADEK873124ANCHOR BIOPSY NEEDLEK790405ANCHOR BRAND COUNT-TAINER

View all 7 devices →

Related Devices (Code: GAB)

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.

K012199DIGICAPHumana USA, Inc.K980988AXYA MEDICAL, INC. AUTOMATIC SUTURING AND LIGATING SYSTEM-(ASLS)Axya Medical, Inc.K932591ENDO-JUDGESynergistic Medical Technologies, Inc.K895681CONTRAST BACKGROUND MATERIALApplied Medical TechnologiesK863595COATED SUTURE NEEDLESharpoint, Inc.K812444RADIATION STERILIZATION FOR NEEDLE CNTRDevon Industries, 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.

↑