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FDA 510(k)

NET STRETCHER PAD (TM)

K-Number: K892892 · 1989-11-21

ApplicantNorth East Technology
Decision Date1989-11-21
Product CodeFPP
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

NET STRETCHER PAD (TM) is the device name listed in this FDA 510(k) record. The listed applicant is North East Technology. It received FDA 510(k) clearance on 1989-11-21 under 510(k) number K892892. The device is classified under product code FPP. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the NET STRETCHER PAD (TM)?

NET STRETCHER PAD (TM) is a medical device that received FDA 510(k) clearance on 1989-11-21. The listed applicant is North East Technology. The 510(k) number is K892892.

When did NET STRETCHER PAD (TM) receive FDA 510(k) clearance?

NET STRETCHER PAD (TM) received FDA 510(k) clearance on 1989-11-21, under 510(k) number K892892.

Who is the listed applicant for NET STRETCHER PAD (TM)?

The FDA 510(k) record lists North East Technology as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for NET STRETCHER PAD (TM)?

The FDA product code for NET STRETCHER PAD (TM) is FPP.

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 North East Technology 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.

K892890STETH-SHIELD(TM)

Related Devices (Code: FPP)

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.

K030283BABY PODPrism Enterprises, Inc.K942356MED-EVAC-4 MEDICAL EVACUATION STRETCHERMontery Bay Corp.K940130STRYKER MODEL 6110 EMERGENCY/POLE STRETCHERStryker Corp.K940245EVACU-SLEDEvacu Technologies, Inc.K924275RESTRAINING STRETCHERDmsK922816U P CUSTOM DESIGN, INC. COT EQUIPMENT CARRIERUp Custom Design, 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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