REMOVAWELL PLATE LID
K-Number: K823557 · 1982-12-28
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Device Summary
Frequently Asked Questions
What is the REMOVAWELL PLATE LID?
REMOVAWELL PLATE LID is a medical device that received FDA 510(k) clearance on 1982-12-28. The listed applicant is Dynatech Corp.. The 510(k) number is K823557.
When did REMOVAWELL PLATE LID receive FDA 510(k) clearance?
REMOVAWELL PLATE LID received FDA 510(k) clearance on 1982-12-28, under 510(k) number K823557.
Who is the listed applicant for REMOVAWELL PLATE LID?
The FDA 510(k) record lists Dynatech Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for REMOVAWELL PLATE LID?
The FDA product code for REMOVAWELL PLATE LID is LIB.
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 Dynatech 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: LIB)
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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