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)

DEVIN-NESTOR SQUARE KNIFE

K-Number: K780989 · 1978-10-03

ApplicantNestor Engineering Associates, Inc.
Decision Date1978-10-03
Product CodeEMF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

DEVIN-NESTOR SQUARE KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Nestor Engineering Associates, Inc.. It received FDA 510(k) clearance on 1978-10-03 under 510(k) number K780989. The device is classified under product code EMF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DEVIN-NESTOR SQUARE KNIFE?

DEVIN-NESTOR SQUARE KNIFE is a medical device that received FDA 510(k) clearance on 1978-10-03. The listed applicant is Nestor Engineering Associates, Inc.. The 510(k) number is K780989.

When did DEVIN-NESTOR SQUARE KNIFE receive FDA 510(k) clearance?

DEVIN-NESTOR SQUARE KNIFE received FDA 510(k) clearance on 1978-10-03, under 510(k) number K780989.

Who is the listed applicant for DEVIN-NESTOR SQUARE KNIFE?

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

What is the FDA product code for DEVIN-NESTOR SQUARE KNIFE?

The FDA product code for DEVIN-NESTOR SQUARE KNIFE is EMF.

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 Nestor Engineering Associates, 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.

K780990STAINLESS STEEL TEMPLATEK780988DEVIN-NESTOR PNEUMATIC TOURNIQUETK780991PARALLEL BLADE MARKERK780992MILLARD MOUTH GAG

Related Devices (Code: EMF)

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.

K080133MOUNTABLE ENDOSCOPIC BLADEA.M. Surgical, Inc.K982142MOUNTABLE ENDOSCOPIC KNIFEA.M. Surgical, Inc.K890215MICROSURGICAL SCARIFIERKinetic Medical ProductsK890217MICROSURGICAL KNIVESKinetic Medical ProductsK890214MICROSURGERY RAZOR BLADE HOLDERKinetic Medical ProductsK880094VAN-TEC ENDOPYELOTOMY KNIFEVan-Tec, 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.

↑