ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION
K-Number: K933051 · 1993-10-12
Advertisement
Device Summary
Frequently Asked Questions
What is the ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION?
ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION is a medical device that received FDA 510(k) clearance on 1993-10-12. The listed applicant is General Components Intl., Inc.. The 510(k) number is K933051.
When did ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION receive FDA 510(k) clearance?
ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION received FDA 510(k) clearance on 1993-10-12, under 510(k) number K933051.
Who is the listed applicant for ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION?
The FDA 510(k) record lists General Components Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION?
The FDA product code for ZERO GRAVITY WHEELCHAIR COMPONENTS, MODIFICATION is KNN.
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 General Components Intl., 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: KNN)
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.
Advertisement