PUTTY, ACCOE
K-Number: K760225 · 1976-07-21
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Device Summary
Frequently Asked Questions
What is the PUTTY, ACCOE?
PUTTY, ACCOE is a medical device that received FDA 510(k) clearance on 1976-07-21. The listed applicant is Coe Laboratories, Inc.. The 510(k) number is K760225.
When did PUTTY, ACCOE receive FDA 510(k) clearance?
PUTTY, ACCOE received FDA 510(k) clearance on 1976-07-21, under 510(k) number K760225.
Who is the listed applicant for PUTTY, ACCOE?
The FDA 510(k) record lists Coe Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for PUTTY, ACCOE?
The FDA product code for PUTTY, ACCOE is ELW.
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 Coe Laboratories, 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: ELW)
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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