7.5 MHZ ENDOVAGINAL PROBE
K-Number: K870709 · 1987-03-27
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Device Summary
Frequently Asked Questions
What is the 7.5 MHZ ENDOVAGINAL PROBE?
7.5 MHZ ENDOVAGINAL PROBE is a medical device that received FDA 510(k) clearance on 1987-03-27. The listed applicant is Philips Ultrasound, Inc.. The 510(k) number is K870709.
When did 7.5 MHZ ENDOVAGINAL PROBE receive FDA 510(k) clearance?
7.5 MHZ ENDOVAGINAL PROBE received FDA 510(k) clearance on 1987-03-27, under 510(k) number K870709.
Who is the listed applicant for 7.5 MHZ ENDOVAGINAL PROBE?
The FDA 510(k) record lists Philips Ultrasound, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for 7.5 MHZ ENDOVAGINAL PROBE?
The FDA product code for 7.5 MHZ ENDOVAGINAL PROBE is HGL.
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 Philips Ultrasound, 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: HGL)
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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