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FDA 510(k)

TRANSVAGINAL TRANSDUCER, 5MHZ

K-Number: K860234 · 1986-05-23

Decision Date1986-05-23
Product CodeHGL
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

TRANSVAGINAL TRANSDUCER, 5MHZ is the device name listed in this FDA 510(k) record. The listed applicant is Philips Medical Systems, Inc.. It received FDA 510(k) clearance on 1986-05-23 under 510(k) number K860234. The device is classified under product code HGL. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TRANSVAGINAL TRANSDUCER, 5MHZ?

TRANSVAGINAL TRANSDUCER, 5MHZ is a medical device that received FDA 510(k) clearance on 1986-05-23. The listed applicant is Philips Medical Systems, Inc.. The 510(k) number is K860234.

When did TRANSVAGINAL TRANSDUCER, 5MHZ receive FDA 510(k) clearance?

TRANSVAGINAL TRANSDUCER, 5MHZ received FDA 510(k) clearance on 1986-05-23, under 510(k) number K860234.

Who is the listed applicant for TRANSVAGINAL TRANSDUCER, 5MHZ?

The FDA 510(k) record lists Philips Medical Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TRANSVAGINAL TRANSDUCER, 5MHZ?

The FDA product code for TRANSVAGINAL TRANSDUCER, 5MHZ 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 Medical Systems, 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.

View all 111 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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