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FDA 510(k)

SUTUREMATE

K-Number: K926126 · 1993-05-19

ApplicantSurgical Safety Products, Inc.
Decision Date1993-05-19
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

SUTUREMATE is the device name listed in this FDA 510(k) record. The listed applicant is Surgical Safety Products, Inc.. It received FDA 510(k) clearance on 1993-05-19 under 510(k) number K926126. The device is classified under product code MDM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SUTUREMATE?

SUTUREMATE is a medical device that received FDA 510(k) clearance on 1993-05-19. The listed applicant is Surgical Safety Products, Inc.. The 510(k) number is K926126.

When did SUTUREMATE receive FDA 510(k) clearance?

SUTUREMATE received FDA 510(k) clearance on 1993-05-19, under 510(k) number K926126.

Who is the listed applicant for SUTUREMATE?

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

What is the FDA product code for SUTUREMATE?

The FDA product code for SUTUREMATE is MDM.

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: MDM)

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.

K073664FRONTLINE MEDICAL SAFETYNET GUIDEWIRE INTRODUCERInjectimed, Inc.K050575FUTUMEDS NO PATIENT CONTACT SAFETY LANCET WITH PALS SYSTEMFutumeds Sdn BhdK050957EUTROCHARSpecial Devices, Inc.K023173ANDREWS INTRODUCER, MODEL ASI01Andrews Surgical Innovations, Ltd.K022059MICROVASIVE PULMONARY GUIDEWIREBoston Scientific CorpK013040LIGHT SABER INTRODUCER NEEDLEMinrad, 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.

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