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FDA 510(k)

INTRAUTERINE CATHETER TIP

K-Number: K790678 · 1979-05-11

Decision Date1979-05-11
Product CodeKXO
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

INTRAUTERINE CATHETER TIP is the device name listed in this FDA 510(k) record. The listed applicant is Sonicaid, Inc.. It received FDA 510(k) clearance on 1979-05-11 under 510(k) number K790678. The device is classified under product code KXO. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INTRAUTERINE CATHETER TIP?

INTRAUTERINE CATHETER TIP is a medical device that received FDA 510(k) clearance on 1979-05-11. The listed applicant is Sonicaid, Inc.. The 510(k) number is K790678.

When did INTRAUTERINE CATHETER TIP receive FDA 510(k) clearance?

INTRAUTERINE CATHETER TIP received FDA 510(k) clearance on 1979-05-11, under 510(k) number K790678.

Who is the listed applicant for INTRAUTERINE CATHETER TIP?

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

What is the FDA product code for INTRAUTERINE CATHETER TIP?

The FDA product code for INTRAUTERINE CATHETER TIP is KXO.

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 Sonicaid, 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 18 devices →

Related Devices (Code: KXO)

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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