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FDA 510(k)

PANORAMIC X-RAY SYSTEM MODEL A

K-Number: K772164 · 1977-12-02

ApplicantSybron Corp.
Decision Date1977-12-02
Product CodeEHD
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

PANORAMIC X-RAY SYSTEM MODEL A is the device name listed in this FDA 510(k) record. The listed applicant is Sybron Corp.. It received FDA 510(k) clearance on 1977-12-02 under 510(k) number K772164. 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 SYSTEM MODEL A?

PANORAMIC X-RAY SYSTEM MODEL A is a medical device that received FDA 510(k) clearance on 1977-12-02. The listed applicant is Sybron Corp.. The 510(k) number is K772164.

When did PANORAMIC X-RAY SYSTEM MODEL A receive FDA 510(k) clearance?

PANORAMIC X-RAY SYSTEM MODEL A received FDA 510(k) clearance on 1977-12-02, under 510(k) number K772164.

Who is the listed applicant for PANORAMIC X-RAY SYSTEM MODEL A?

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

What is the FDA product code for PANORAMIC X-RAY SYSTEM MODEL A?

The FDA product code for PANORAMIC X-RAY SYSTEM MODEL A 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 Sybron 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.

View all 37 devices →

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.

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