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)

PANORAMIC X-RAY MODEL PC-1000

K-Number: K870236 · 1987-02-13

Decision Date1987-02-13
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANORAMIC X-RAY MODEL PC-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 1987-02-13 under 510(k) number K870236. 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 PANORAMIC X-RAY MODEL PC-1000?

PANORAMIC X-RAY MODEL PC-1000 is a medical device that received FDA 510(k) clearance on 1987-02-13. The listed applicant is Panoramic Corp.. The 510(k) number is K870236.

When did PANORAMIC X-RAY MODEL PC-1000 receive FDA 510(k) clearance?

PANORAMIC X-RAY MODEL PC-1000 received FDA 510(k) clearance on 1987-02-13, under 510(k) number K870236.

Who is the listed applicant for PANORAMIC X-RAY MODEL PC-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 PANORAMIC X-RAY MODEL PC-1000?

The FDA product code for PANORAMIC X-RAY MODEL PC-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.

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.

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.

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.

↑