VOLKER NURSING BED MODEL 2080E & 2090E
K-Number: K946208 · 1995-03-14
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Device Summary
Frequently Asked Questions
What is the VOLKER NURSING BED MODEL 2080E & 2090E?
VOLKER NURSING BED MODEL 2080E & 2090E is a medical device that received FDA 510(k) clearance on 1995-03-14. The listed applicant is Volker Healthcare, Inc.. The 510(k) number is K946208.
When did VOLKER NURSING BED MODEL 2080E & 2090E receive FDA 510(k) clearance?
VOLKER NURSING BED MODEL 2080E & 2090E received FDA 510(k) clearance on 1995-03-14, under 510(k) number K946208.
Who is the listed applicant for VOLKER NURSING BED MODEL 2080E & 2090E?
The FDA 510(k) record lists Volker Healthcare, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for VOLKER NURSING BED MODEL 2080E & 2090E?
The FDA product code for VOLKER NURSING BED MODEL 2080E & 2090E is FNL.
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 Volker Healthcare, 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: FNL)
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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