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)

VAIL 1000 ENCLOSED BED

K-Number: K982783 · 1998-10-05

Decision Date1998-10-05
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

VAIL 1000 ENCLOSED BED is the device name listed in this FDA 510(k) record. The listed applicant is Vail Products, Inc.. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982783. 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 VAIL 1000 ENCLOSED BED?

VAIL 1000 ENCLOSED BED is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Vail Products, Inc.. The 510(k) number is K982783.

When did VAIL 1000 ENCLOSED BED receive FDA 510(k) clearance?

VAIL 1000 ENCLOSED BED received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982783.

Who is the listed applicant for VAIL 1000 ENCLOSED BED?

The FDA 510(k) record lists Vail Products, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for VAIL 1000 ENCLOSED BED?

The FDA product code for VAIL 1000 ENCLOSED BED 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 Vail Products, 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.

↑