Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

MYLAR WINDOW-TABLE INSERT PANEL

K-Number: K800791 · 1980-05-14

ApplicantRadiation Products Design, Inc.
Decision Date1980-05-14
Product CodeIYE
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MYLAR WINDOW-TABLE INSERT PANEL is the device name listed in this FDA 510(k) record. The listed applicant is Radiation Products Design, Inc.. It received FDA 510(k) clearance on 1980-05-14 under 510(k) number K800791. The device is classified under product code IYE. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYLAR WINDOW-TABLE INSERT PANEL?

MYLAR WINDOW-TABLE INSERT PANEL is a medical device that received FDA 510(k) clearance on 1980-05-14. The listed applicant is Radiation Products Design, Inc.. The 510(k) number is K800791.

When did MYLAR WINDOW-TABLE INSERT PANEL receive FDA 510(k) clearance?

MYLAR WINDOW-TABLE INSERT PANEL received FDA 510(k) clearance on 1980-05-14, under 510(k) number K800791.

Who is the listed applicant for MYLAR WINDOW-TABLE INSERT PANEL?

The FDA 510(k) record lists Radiation Products Design, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MYLAR WINDOW-TABLE INSERT PANEL?

The FDA product code for MYLAR WINDOW-TABLE INSERT PANEL is IYE.

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 Radiation Products Design, 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.

K800760BITE BLOCK SYSTEMK800761POINT TO POINT LEVELK800792ADJUSTABLE HEAD & FACE HOLDERK800790TENNIS RACKET-TABLE INSERT PANELK800759ELEV. BACK SUPPORT W/ADJ. ARM POSITIONERK791178MYVACET 5-07, 7-00 AND 9-40

View all 7 devices →

Related Devices (Code: IYE)

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.

K261865AerFrame™ Alignment Laser Box (LBV2)Stabilix, LLCK261718EZFluence (RADEZ V2)Radformation, Inc.K260733MRIA Radiation Therapy Information System (MRIA)Manteia Technologies Co., Ltd.K261856Halcyon, Ethos Radiotherapy System (5.0)Varian Medical Systems, Inc.K252937ThinkQA 3Dosisoft SAK253004LUNA 3DLap GmbH Laser Applikationen

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.

↑