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)

FLEXON AND STAINLESS STEEL SUTURES

K-Number: K930992 · 1993-12-17

ApplicantAmerican Cyanamid Co.
Decision Date1993-12-17
Product CodeGAQ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

FLEXON AND STAINLESS STEEL SUTURES is the device name listed in this FDA 510(k) record. The listed applicant is American Cyanamid Co.. It received FDA 510(k) clearance on 1993-12-17 under 510(k) number K930992. The device is classified under product code GAQ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FLEXON AND STAINLESS STEEL SUTURES?

FLEXON AND STAINLESS STEEL SUTURES is a medical device that received FDA 510(k) clearance on 1993-12-17. The listed applicant is American Cyanamid Co.. The 510(k) number is K930992.

When did FLEXON AND STAINLESS STEEL SUTURES receive FDA 510(k) clearance?

FLEXON AND STAINLESS STEEL SUTURES received FDA 510(k) clearance on 1993-12-17, under 510(k) number K930992.

Who is the listed applicant for FLEXON AND STAINLESS STEEL SUTURES?

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

What is the FDA product code for FLEXON AND STAINLESS STEEL SUTURES?

The FDA product code for FLEXON AND STAINLESS STEEL SUTURES is GAQ.

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 American Cyanamid 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.

K931056DAVIS+GECK VALTRAC BIOFRAG ANASTOMOSIS RINGK921696CUTTING AND COAGULATION DEVICES AND ACCESSORIESK922348VALTRAC(R) INTRODUCER FORCEPK900198DEXON II ABSORBABLE SURGICAL SUTURE, U.S.P.K896946COATED NOVAFIL, POLYBUTESTER, MESHK823552APPOSE SKIN STAPLER & REMOVER

View all 7 devices →

Related Devices (Code: GAQ)

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.

K203855CoNextions TR Tendon Repair SystemConextions MedicalK193209Wego-Stainless SteelFoosin Medical Supplies Inc., Ltd.K172146MERISTEELM/s. Meril Endo Surgery Private Limited.K170767Surgical Stainless Steel Suture, Stainless Steel SutureETHICON, Inc.K081060FERROFIBRE STAINLESS STEEL SUTURES, MODEL 610 SERIES SIZES (USP) 5-0 TO #5Core Essence Orthopaedics, LLCK082828SUTURTEK 360 DEGREE STERNAL CLOSURE DEVICESuturtek Incorporated

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.

↑