AMP BUFFER
K-Number: K760410 · 1976-10-29
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Device Summary
Frequently Asked Questions
What is the AMP BUFFER?
AMP BUFFER is a medical device that received FDA 510(k) clearance on 1976-10-29. The listed applicant is J.T. Baker Chemical Co.. The 510(k) number is K760410.
When did AMP BUFFER receive FDA 510(k) clearance?
AMP BUFFER received FDA 510(k) clearance on 1976-10-29, under 510(k) number K760410.
Who is the listed applicant for AMP BUFFER?
The FDA 510(k) record lists J.T. Baker Chemical Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for AMP BUFFER?
The FDA product code for AMP BUFFER is CFJ.
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 J.T. Baker Chemical Co. 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: CFJ)
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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