GC-1000 THROUGH GC-3005 ACID CONCENTRATE
K-Number: K901471 · 1990-07-27
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Device Summary
Frequently Asked Questions
What is the GC-1000 THROUGH GC-3005 ACID CONCENTRATE?
GC-1000 THROUGH GC-3005 ACID CONCENTRATE is a medical device that received FDA 510(k) clearance on 1990-07-27. The listed applicant is Granite Chemical Co., Inc.. The 510(k) number is K901471.
When did GC-1000 THROUGH GC-3005 ACID CONCENTRATE receive FDA 510(k) clearance?
GC-1000 THROUGH GC-3005 ACID CONCENTRATE received FDA 510(k) clearance on 1990-07-27, under 510(k) number K901471.
Who is the listed applicant for GC-1000 THROUGH GC-3005 ACID CONCENTRATE?
The FDA 510(k) record lists Granite Chemical Co., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GC-1000 THROUGH GC-3005 ACID CONCENTRATE?
The FDA product code for GC-1000 THROUGH GC-3005 ACID CONCENTRATE is KPO.
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 Granite Chemical Co., 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: KPO)
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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