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FDA 510(k)

TKO TELESCOPING LITHOTOMY STIRRUP

K-Number: K904826 · 1990-10-31

ApplicantD.L. Nelson and Assoc., Inc.
Decision Date1990-10-31
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

TKO TELESCOPING LITHOTOMY STIRRUP is the device name listed in this FDA 510(k) record. The listed applicant is D.L. Nelson and Assoc., Inc.. It received FDA 510(k) clearance on 1990-10-31 under 510(k) number K904826. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TKO TELESCOPING LITHOTOMY STIRRUP?

TKO TELESCOPING LITHOTOMY STIRRUP is a medical device that received FDA 510(k) clearance on 1990-10-31. The listed applicant is D.L. Nelson and Assoc., Inc.. The 510(k) number is K904826.

When did TKO TELESCOPING LITHOTOMY STIRRUP receive FDA 510(k) clearance?

TKO TELESCOPING LITHOTOMY STIRRUP received FDA 510(k) clearance on 1990-10-31, under 510(k) number K904826.

Who is the listed applicant for TKO TELESCOPING LITHOTOMY STIRRUP?

The FDA 510(k) record lists D.L. Nelson and Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TKO TELESCOPING LITHOTOMY STIRRUP?

The FDA product code for TKO TELESCOPING LITHOTOMY STIRRUP is FWZ.

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 D.L. Nelson and Assoc., 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.

K944238ENDOCYTE TMK945415'LIL MAC ACCESSORY CLAMP(TM)K925035MIDKIFF GEOSTATIC CLAMP

Related Devices (Code: FWZ)

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.

K960019RETRACTOR ARM CLAMPBiopsys Medical, Inc.K945415'LIL MAC ACCESSORY CLAMP(TM)D.L. Nelson and Assoc., Inc.K944779CARBON LIGHTS HAND SURGERY TABLEAllen Medical Systems, Inc.K935381KAPS POSITIONING ARMAndronic Devices, Ltd.K931037WHITMORE VACUUM-LOCK SPINAL FRAME (VLSF-100)Whitmore Ent., Inc.K926225SPONGE COUNTERAmerican Medical Manufacturer, 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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