INTRAUTERINE SOUND, PLASTIC DISPOSABLE
K-Number: K760170 · 1976-07-19
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Device Summary
Frequently Asked Questions
What is the INTRAUTERINE SOUND, PLASTIC DISPOSABLE?
INTRAUTERINE SOUND, PLASTIC DISPOSABLE is a medical device that received FDA 510(k) clearance on 1976-07-19. The listed applicant is G.D. Searle and Co.. The 510(k) number is K760170.
When did INTRAUTERINE SOUND, PLASTIC DISPOSABLE receive FDA 510(k) clearance?
INTRAUTERINE SOUND, PLASTIC DISPOSABLE received FDA 510(k) clearance on 1976-07-19, under 510(k) number K760170.
Who is the listed applicant for INTRAUTERINE SOUND, PLASTIC DISPOSABLE?
The FDA 510(k) record lists G.D. Searle and Co. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for INTRAUTERINE SOUND, PLASTIC DISPOSABLE?
The FDA product code for INTRAUTERINE SOUND, PLASTIC DISPOSABLE 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 G.D. Searle and Co. 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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