DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES
K-Number: K954847 · 1996-05-22
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Device Summary
Frequently Asked Questions
What is the DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES?
DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES is a medical device that received FDA 510(k) clearance on 1996-05-22. The listed applicant is Ocg Systems, Inc.. The 510(k) number is K954847.
When did DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES receive FDA 510(k) clearance?
DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES received FDA 510(k) clearance on 1996-05-22, under 510(k) number K954847.
Who is the listed applicant for DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES?
The FDA 510(k) record lists Ocg Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES?
The FDA product code for DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIES is HFM.
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.
Related Devices (Code: HFM)
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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