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)

MOMENTUM NO. FS008 WHEELCHAIR

K-Number: K982099 · 1998-10-05

Decision Date1998-10-05
Product CodeIOR
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

MOMENTUM NO. FS008 WHEELCHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Sriram Enterprises D.B.A. Momentum Group. It received FDA 510(k) clearance on 1998-10-05 under 510(k) number K982099. 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 MOMENTUM NO. FS008 WHEELCHAIR?

MOMENTUM NO. FS008 WHEELCHAIR is a medical device that received FDA 510(k) clearance on 1998-10-05. The listed applicant is Sriram Enterprises D.B.A. Momentum Group. The 510(k) number is K982099.

When did MOMENTUM NO. FS008 WHEELCHAIR receive FDA 510(k) clearance?

MOMENTUM NO. FS008 WHEELCHAIR received FDA 510(k) clearance on 1998-10-05, under 510(k) number K982099.

Who is the listed applicant for MOMENTUM NO. FS008 WHEELCHAIR?

The FDA 510(k) record lists Sriram Enterprises D.B.A. Momentum Group as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for MOMENTUM NO. FS008 WHEELCHAIR?

The FDA product code for MOMENTUM NO. FS008 WHEELCHAIR 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.

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.

↑