PLANAR DOME EX LINE MODEL DOME E2C
K-Number: K061018 · 2006-04-28
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Device Summary
Frequently Asked Questions
What is the PLANAR DOME EX LINE MODEL DOME E2C?
PLANAR DOME EX LINE MODEL DOME E2C is a medical device that received FDA 510(k) clearance on 2006-04-28. The listed applicant is Planar Systems, Inc.. The 510(k) number is K061018.
When did PLANAR DOME EX LINE MODEL DOME E2C receive FDA 510(k) clearance?
PLANAR DOME EX LINE MODEL DOME E2C received FDA 510(k) clearance on 2006-04-28, under 510(k) number K061018.
Who is the listed applicant for PLANAR DOME EX LINE MODEL DOME E2C?
The FDA 510(k) record lists Planar Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PLANAR DOME EX LINE MODEL DOME E2C?
The FDA product code for PLANAR DOME EX LINE MODEL DOME E2C is LLZ.
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 Planar Systems, Inc. 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: 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.
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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