Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

VOLKER NURSING BED MODEL 2080E & 2090E

K-Number: K946208 · 1995-03-14

Decision Date1995-03-14
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VOLKER NURSING BED MODEL 2080E & 2090E is the device name listed in this FDA 510(k) record. The listed applicant is Volker Healthcare, Inc.. It received FDA 510(k) clearance on 1995-03-14 under 510(k) number K946208. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

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.

↑