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)

PREP AND OPERATING STAND

K-Number: K905564 · 1991-02-21

Decision Date1991-02-21
Product CodeFWZ
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PREP AND OPERATING STAND is the device name listed in this FDA 510(k) record. The listed applicant is Mcconnell Orthopedic. It received FDA 510(k) clearance on 1991-02-21 under 510(k) number K905564. The device is classified under product code FWZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREP AND OPERATING STAND?

PREP AND OPERATING STAND is a medical device that received FDA 510(k) clearance on 1991-02-21. The listed applicant is Mcconnell Orthopedic. The 510(k) number is K905564.

When did PREP AND OPERATING STAND receive FDA 510(k) clearance?

PREP AND OPERATING STAND received FDA 510(k) clearance on 1991-02-21, under 510(k) number K905564.

Who is the listed applicant for PREP AND OPERATING STAND?

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

What is the FDA product code for PREP AND OPERATING STAND?

The FDA product code for PREP AND OPERATING STAND is FWZ.

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 Mcconnell Orthopedic 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 16 devices →

Related Devices (Code: FWZ)

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.

↑