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FDA 510(k)

PMD VIEWER

K-Number: K092204 · 2009-10-08

ApplicantSpencer Technologies
Decision Date2009-10-08
Product CodeLLZ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

PMD VIEWER is the device name listed in this FDA 510(k) record. The listed applicant is Spencer Technologies. It received FDA 510(k) clearance on 2009-10-08 under 510(k) number K092204. The device is classified under product code LLZ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PMD VIEWER?

PMD VIEWER is a medical device that received FDA 510(k) clearance on 2009-10-08. The listed applicant is Spencer Technologies. The 510(k) number is K092204.

When did PMD VIEWER receive FDA 510(k) clearance?

PMD VIEWER received FDA 510(k) clearance on 2009-10-08, under 510(k) number K092204.

Who is the listed applicant for PMD VIEWER?

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

What is the FDA product code for PMD VIEWER?

The FDA product code for PMD VIEWER is LLZ.

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Other records listing Spencer Technologies 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.

K002533TCD 100M, PWD13 TRANSDUCER

Related Devices (Code: LLZ)

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.

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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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