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FDA 510(k)

LEADED X-RAY APRON

K-Number: K832601 · 1983-09-29

ApplicantE.M. Adams
Decision Date1983-09-29
Product CodeEAJ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

LEADED X-RAY APRON is the device name listed in this FDA 510(k) record. The listed applicant is E.M. Adams. It received FDA 510(k) clearance on 1983-09-29 under 510(k) number K832601. The device is classified under product code EAJ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LEADED X-RAY APRON?

LEADED X-RAY APRON is a medical device that received FDA 510(k) clearance on 1983-09-29. The listed applicant is E.M. Adams. The 510(k) number is K832601.

When did LEADED X-RAY APRON receive FDA 510(k) clearance?

LEADED X-RAY APRON received FDA 510(k) clearance on 1983-09-29, under 510(k) number K832601.

Who is the listed applicant for LEADED X-RAY APRON?

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

What is the FDA product code for LEADED X-RAY APRON?

The FDA product code for LEADED X-RAY APRON is EAJ.

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 E.M. Adams 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.

K905173SPLASH GUARDK910468STERILE DISPOSABLE DRAPE(S)K873978DISPOSABLE BIPOLAR FORCEPSK850063INSTRUMENT POCKETK843724I.V. START KIT & OBSTETRICAL KITK843783WET PACK

View all 21 devices →

Related Devices (Code: EAJ)

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.

K931269LEAD APRONBt Medical Co., Inc.K913621RINN PROTECTIVE X-RAY APRON AND PROTECTIVE COLLARRinn Dental ProductsK870563X-RAY APRONX-Tech, Ltd.K870103LEAD APRON CADDYOrthopedic Systems, Inc.K832602THYROID PROTECTIVE COLLARE.M. Adams

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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