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)

LASER - 1000

K-Number: K882436 · 1988-08-04

ApplicantPanoramic Corp.
Decision Date1988-08-04
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

LASER - 1000 is the device name listed in this FDA 510(k) record. The listed applicant is Panoramic Corp.. It received FDA 510(k) clearance on 1988-08-04 under 510(k) number K882436. The device is classified under product code EHD. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER - 1000?

LASER - 1000 is a medical device that received FDA 510(k) clearance on 1988-08-04. The listed applicant is Panoramic Corp.. The 510(k) number is K882436.

When did LASER - 1000 receive FDA 510(k) clearance?

LASER - 1000 received FDA 510(k) clearance on 1988-08-04, under 510(k) number K882436.

Who is the listed applicant for LASER - 1000?

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

What is the FDA product code for LASER - 1000?

The FDA product code for LASER - 1000 is EHD.

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 Panoramic Corp. 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.

K152489ENCOMPASS Eagle 3D CBCT/Panoramic/Cephalometric Dental X-RayK110371ENCOMPASS HF100- EAGLE PANORAMIC/CEPHALOMETRIC X-RAYK043557MODEL PC-1000 PANORAMIC/CEPHALOMETRIC X-RAY SYSTEMSK943532PANORAMIC CORPORATION HDLXK870236PANORAMIC X-RAY MODEL PC-1000

Related Devices (Code: EHD)

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.

K260795Hand-held Dental X-ray System (HyperLight-M)Changzhou Sifary Medical Technology Co., Ltd.K260367Portable Dental X-ray System Model PDX novaPDX Co., Ltd.K253864NOMAD Pro 3Dental Imaging Technologies CorporationK252110Dental X-RAY Unit (AJX200)Guangzhou Ajax Medical Equipment Co., Ltd.K254018Portable Dental X-ray Device (GT-1)Guilin Refine Medical Instrument Co., Ltd.K252909Diagnostic X-Ray Equipment Model POCT22Ningbo Runyes Medical Instrument Co., Ltd.

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.

↑