POWER EXAMINATION TABLE MODEL # 411
K-Number: K894134 · 1989-08-28
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Device Summary
Frequently Asked Questions
What is the POWER EXAMINATION TABLE MODEL # 411?
POWER EXAMINATION TABLE MODEL # 411 is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Midmark Corp.. The 510(k) number is K894134.
When did POWER EXAMINATION TABLE MODEL # 411 receive FDA 510(k) clearance?
POWER EXAMINATION TABLE MODEL # 411 received FDA 510(k) clearance on 1989-08-28, under 510(k) number K894134.
Who is the listed applicant for POWER EXAMINATION TABLE MODEL # 411?
The FDA 510(k) record lists Midmark Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for POWER EXAMINATION TABLE MODEL # 411?
The FDA product code for POWER EXAMINATION TABLE MODEL # 411 is LGX.
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 Midmark 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: LGX)
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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