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)

PORTABLE WHEELCHAIR & CARRYING CASE

K-Number: K790183 · 1979-03-21

Decision Date1979-03-21
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

PORTABLE WHEELCHAIR & CARRYING CASE is the device name listed in this FDA 510(k) record. The listed applicant is Fred Sammons, Inc.. It received FDA 510(k) clearance on 1979-03-21 under 510(k) number K790183. The device is classified under product code IOR. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PORTABLE WHEELCHAIR & CARRYING CASE?

PORTABLE WHEELCHAIR & CARRYING CASE is a medical device that received FDA 510(k) clearance on 1979-03-21. The listed applicant is Fred Sammons, Inc.. The 510(k) number is K790183.

When did PORTABLE WHEELCHAIR & CARRYING CASE receive FDA 510(k) clearance?

PORTABLE WHEELCHAIR & CARRYING CASE received FDA 510(k) clearance on 1979-03-21, under 510(k) number K790183.

Who is the listed applicant for PORTABLE WHEELCHAIR & CARRYING CASE?

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

What is the FDA product code for PORTABLE WHEELCHAIR & CARRYING CASE?

The FDA product code for PORTABLE WHEELCHAIR & CARRYING CASE is IOR.

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 Fred Sammons, 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.

View all 278 devices →

Related Devices (Code: IOR)

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.

↑