COLLECTOR, SANI-CATCH, NO. 1014
K-Number: K770673 · 1977-04-15
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Device Summary
Frequently Asked Questions
What is the COLLECTOR, SANI-CATCH, NO. 1014?
COLLECTOR, SANI-CATCH, NO. 1014 is a medical device that received FDA 510(k) clearance on 1977-04-15. The listed applicant is Concord Laboratories, Inc.. The 510(k) number is K770673.
When did COLLECTOR, SANI-CATCH, NO. 1014 receive FDA 510(k) clearance?
COLLECTOR, SANI-CATCH, NO. 1014 received FDA 510(k) clearance on 1977-04-15, under 510(k) number K770673.
Who is the listed applicant for COLLECTOR, SANI-CATCH, NO. 1014?
The FDA 510(k) record lists Concord Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for COLLECTOR, SANI-CATCH, NO. 1014?
The FDA product code for COLLECTOR, SANI-CATCH, NO. 1014 is KNX.
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 Concord 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: KNX)
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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