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FDA 510(k)

KITS AND TRAYS FOR ONE TIME USE ONLY

K-Number: K903963 · 1991-07-29

ApplicantApk Technology
Decision Date1991-07-29
Product CodeLRP
Advisory CommitteeSU
DecisionUnknown

Device Summary

KITS AND TRAYS FOR ONE TIME USE ONLY is the device name listed in this FDA 510(k) record. The listed applicant is Apk Technology. It received FDA 510(k) clearance on 1991-07-29 under 510(k) number K903963. The device is classified under product code LRP. It was reviewed by the SU advisory panel. FDA Decision: Unknown.

Frequently Asked Questions

What is the KITS AND TRAYS FOR ONE TIME USE ONLY?

KITS AND TRAYS FOR ONE TIME USE ONLY is a medical device that received FDA 510(k) clearance on 1991-07-29. The listed applicant is Apk Technology. The 510(k) number is K903963.

When did KITS AND TRAYS FOR ONE TIME USE ONLY receive FDA 510(k) clearance?

KITS AND TRAYS FOR ONE TIME USE ONLY received FDA 510(k) clearance on 1991-07-29, under 510(k) number K903963.

Who is the listed applicant for KITS AND TRAYS FOR ONE TIME USE ONLY?

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

What is the FDA product code for KITS AND TRAYS FOR ONE TIME USE ONLY?

The FDA product code for KITS AND TRAYS FOR ONE TIME USE ONLY is LRP.

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 Apk 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.

K903962INSTRUMENTS FOR ONE TIME USE/ DISPOSABLE

Related Devices (Code: LRP)

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.

K963723LACERATION TRAYGrand Medical ProductsK951811OSTEOTECH MUSCULOSKELETAL TISSUE RECOVERY PACKOsteotech, Inc.K940239EYE TRAYCush Medical ProductsK935621CUSTOM ENT PACKSAssociated MedicalK940646ORTHOPEDIC TRAY PRODUCT LINECushinduK940444GENERAL SURGERY TRAYCush Medical Products

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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