MAGNA OBSTETRICAL PACKS
K-Number: K911509 · 1991-06-17
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Device Summary
Frequently Asked Questions
What is the MAGNA OBSTETRICAL PACKS?
MAGNA OBSTETRICAL PACKS is a medical device that received FDA 510(k) clearance on 1991-06-17. The listed applicant is Dms Miami, Inc.. The 510(k) number is K911509.
When did MAGNA OBSTETRICAL PACKS receive FDA 510(k) clearance?
MAGNA OBSTETRICAL PACKS received FDA 510(k) clearance on 1991-06-17, under 510(k) number K911509.
Who is the listed applicant for MAGNA OBSTETRICAL PACKS?
The FDA 510(k) record lists Dms Miami, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for MAGNA OBSTETRICAL PACKS?
The FDA product code for MAGNA OBSTETRICAL PACKS is KKX.
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 Dms Miami, 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: KKX)
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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