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FDA 510(k)

SAFETY RELEASE MODULE

K-Number: K961754 · 1996-07-10

ApplicantG & H Wire Co.
Decision Date1996-07-10
Product CodeDZB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

SAFETY RELEASE MODULE is the device name listed in this FDA 510(k) record. The listed applicant is G & H Wire Co.. It received FDA 510(k) clearance on 1996-07-10 under 510(k) number K961754. The device is classified under product code DZB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SAFETY RELEASE MODULE?

SAFETY RELEASE MODULE is a medical device that received FDA 510(k) clearance on 1996-07-10. The listed applicant is G & H Wire Co.. The 510(k) number is K961754.

When did SAFETY RELEASE MODULE receive FDA 510(k) clearance?

SAFETY RELEASE MODULE received FDA 510(k) clearance on 1996-07-10, under 510(k) number K961754.

Who is the listed applicant for SAFETY RELEASE MODULE?

The FDA 510(k) record lists G & H Wire Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SAFETY RELEASE MODULE?

The FDA product code for SAFETY RELEASE MODULE is DZB.

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 G & H Wire 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.

K081393ORTHODONTIC TEMPORARY ANCHORAGE IMPLANT SCREW

Related Devices (Code: DZB)

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.

K202855Orthodontic FacemaskIta.O Italian Orthodontic System S.R.L.K162543Reverse Pull Adjustable FacemaskSawbros Industries Pvt., Ltd.K111169PROTRACTION FACE MASK, REVERSE PULL FACE MASK MODEL KM-PVS, KM-PIS, KM-PVM, KM-PIM, MODEL KM-FMS, KM-FML, KM-FMFKwang Myung Daicom, Inc.K103019KJ MASKKj Meditech Co., Ltd.K052553NITOM LOCKING FACEBOWRussell Samuels Orthodontic DesignK051751EQUA-PULL SAFETY RELEASE MODULEOrtho Technology

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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