1208 BETACORD AND 1208 BETCORD M
K-Number: K852434 · 1985-08-02
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Device Summary
Frequently Asked Questions
What is the 1208 BETACORD AND 1208 BETCORD M?
1208 BETACORD AND 1208 BETCORD M is a medical device that received FDA 510(k) clearance on 1985-08-02. The listed applicant is Lkb Instruments, Inc.. The 510(k) number is K852434.
When did 1208 BETACORD AND 1208 BETCORD M receive FDA 510(k) clearance?
1208 BETACORD AND 1208 BETCORD M received FDA 510(k) clearance on 1985-08-02, under 510(k) number K852434.
Who is the listed applicant for 1208 BETACORD AND 1208 BETCORD M?
The FDA 510(k) record lists Lkb Instruments, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 1208 BETACORD AND 1208 BETCORD M?
The FDA product code for 1208 BETACORD AND 1208 BETCORD M is JJJ.
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 Lkb Instruments, 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: JJJ)
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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