GRAVITY ASSIST
K-Number: K902854 · 1990-08-29
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Device Summary
Frequently Asked Questions
What is the GRAVITY ASSIST?
GRAVITY ASSIST is a medical device that received FDA 510(k) clearance on 1990-08-29. The listed applicant is Instrument Makar, Inc.. The 510(k) number is K902854.
When did GRAVITY ASSIST receive FDA 510(k) clearance?
GRAVITY ASSIST received FDA 510(k) clearance on 1990-08-29, under 510(k) number K902854.
Who is the listed applicant for GRAVITY ASSIST?
The FDA 510(k) record lists Instrument Makar, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GRAVITY ASSIST?
The FDA product code for GRAVITY ASSIST is KYZ.
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 Instrument Makar, 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: KYZ)
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.
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