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FDA 510(k)

DEEP SUTURE

K-Number: K942818 · 1994-08-25

ApplicantAutomated Medical Products Corp.
Decision Date1994-08-25
Product CodeMDM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEEP SUTURE is the device name listed in this FDA 510(k) record. The listed applicant is Automated Medical Products Corp.. It received FDA 510(k) clearance on 1994-08-25 under 510(k) number K942818. 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 DEEP SUTURE?

DEEP SUTURE is a medical device that received FDA 510(k) clearance on 1994-08-25. The listed applicant is Automated Medical Products Corp.. The 510(k) number is K942818.

When did DEEP SUTURE receive FDA 510(k) clearance?

DEEP SUTURE received FDA 510(k) clearance on 1994-08-25, under 510(k) number K942818.

Who is the listed applicant for DEEP SUTURE?

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

What is the FDA product code for DEEP SUTURE?

The FDA product code for DEEP SUTURE 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

Other records listing Automated Medical Products Corp. 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.

K942910DEEPVISONK942002RETRACTORK940199DISSECTOR

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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