FDA 510(k)

PANORAMIC CORPORATION HDLX

K-Number: K943532 · 1994-12-07

Decision Date1994-12-07

Product CodeJAA

Advisory CommitteeRA

DecisionSubstantially Equivalent

Device Summary

PANORAMIC CORPORATION HDLX is the device name listed in this FDA 510(k) record. The listed applicant is Panoramic Corp.. It received FDA 510(k) clearance on 1994-12-07 under 510(k) number K943532. The device is classified under product code JAA. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PANORAMIC CORPORATION HDLX?

PANORAMIC CORPORATION HDLX is a medical device that received FDA 510(k) clearance on 1994-12-07. The listed applicant is Panoramic Corp.. The 510(k) number is K943532.

When did PANORAMIC CORPORATION HDLX receive FDA 510(k) clearance?

PANORAMIC CORPORATION HDLX received FDA 510(k) clearance on 1994-12-07, under 510(k) number K943532.

Who is the listed applicant for PANORAMIC CORPORATION HDLX?

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 CORPORATION HDLX?

The FDA product code for PANORAMIC CORPORATION HDLX is JAA.

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Other records listing Panoramic Corp. as applicant

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Related Devices (Code: JAA)

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.