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FDA 510(k)

PDB II VIBRATING DRAINAGE BED

K-Number: K843572 · 1984-11-23

Decision Date1984-11-23
Product CodeJFB
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PDB II VIBRATING DRAINAGE BED is the device name listed in this FDA 510(k) record. The listed applicant is Invacare Corp.. It received FDA 510(k) clearance on 1984-11-23 under 510(k) number K843572. The device is classified under product code JFB. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PDB II VIBRATING DRAINAGE BED?

PDB II VIBRATING DRAINAGE BED is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is Invacare Corp.. The 510(k) number is K843572.

When did PDB II VIBRATING DRAINAGE BED receive FDA 510(k) clearance?

PDB II VIBRATING DRAINAGE BED received FDA 510(k) clearance on 1984-11-23, under 510(k) number K843572.

Who is the listed applicant for PDB II VIBRATING DRAINAGE BED?

The FDA 510(k) record lists Invacare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PDB II VIBRATING DRAINAGE BED?

The FDA product code for PDB II VIBRATING DRAINAGE BED is JFB.

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 Invacare 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.

View all 111 devices →

Related Devices (Code: JFB)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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