OBSTETRICAL BEDS
K-Number: K792568 · 1980-01-28
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Device Summary
Frequently Asked Questions
What is the OBSTETRICAL BEDS?
OBSTETRICAL BEDS is a medical device that received FDA 510(k) clearance on 1980-01-28. The listed applicant is Ets Rene Marzet. The 510(k) number is K792568.
When did OBSTETRICAL BEDS receive FDA 510(k) clearance?
OBSTETRICAL BEDS received FDA 510(k) clearance on 1980-01-28, under 510(k) number K792568.
Who is the listed applicant for OBSTETRICAL BEDS?
The FDA 510(k) record lists Ets Rene Marzet as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for OBSTETRICAL BEDS?
The FDA product code for OBSTETRICAL BEDS 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 Ets Rene Marzet 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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