LIC OBSTETRICAL TABLE
K-Number: K812141 · 1981-08-25
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Device Summary
Frequently Asked Questions
What is the LIC OBSTETRICAL TABLE?
LIC OBSTETRICAL TABLE is a medical device that received FDA 510(k) clearance on 1981-08-25. The listed applicant is Lada Intl., Inc.. The 510(k) number is K812141.
When did LIC OBSTETRICAL TABLE receive FDA 510(k) clearance?
LIC OBSTETRICAL TABLE received FDA 510(k) clearance on 1981-08-25, under 510(k) number K812141.
Who is the listed applicant for LIC OBSTETRICAL TABLE?
The FDA 510(k) record lists Lada Intl., Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LIC OBSTETRICAL TABLE?
The FDA product code for LIC OBSTETRICAL TABLE is KNC.
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 Lada Intl., 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: KNC)
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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