INTRAUTERINE SOUND
K-Number: K935665 · 1994-02-24
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Device Summary
Frequently Asked Questions
What is the INTRAUTERINE SOUND?
INTRAUTERINE SOUND is a medical device that received FDA 510(k) clearance on 1994-02-24. The listed applicant is Rocket of London, Ltd.. The 510(k) number is K935665.
When did INTRAUTERINE SOUND receive FDA 510(k) clearance?
INTRAUTERINE SOUND received FDA 510(k) clearance on 1994-02-24, under 510(k) number K935665.
Who is the listed applicant for INTRAUTERINE SOUND?
The FDA 510(k) record lists Rocket of London, Ltd. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAUTERINE SOUND?
The FDA product code for INTRAUTERINE SOUND is HHM.
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 Rocket of London, Ltd. 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: HHM)
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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