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FDA 510(k)

DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER

K-Number: K920375 · 1992-10-27

ApplicantTelos Medical Corp.
Decision Date1992-10-27
Product CodeHFN
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER is the device name listed in this FDA 510(k) record. The listed applicant is Telos Medical Corp.. It received FDA 510(k) clearance on 1992-10-27 under 510(k) number K920375. The device is classified under product code HFN. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER?

DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER is a medical device that received FDA 510(k) clearance on 1992-10-27. The listed applicant is Telos Medical Corp.. The 510(k) number is K920375.

When did DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER receive FDA 510(k) clearance?

DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER received FDA 510(k) clearance on 1992-10-27, under 510(k) number K920375.

Who is the listed applicant for DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER?

The FDA 510(k) record lists Telos Medical Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER?

The FDA product code for DISPOSABLE INTRAUTERINE PRESSURE TRANSDUCER is HFN.

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Other records listing Telos Medical Corp. 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.

K920044DUAL LUMEN TRANSCERIVICAL INTRAUTERINE KITK914387TRANSCERVICAL INTRAUTERINE KITK905018LAB-SITE SAFETY NEEDLEK905017LAB-SITEK882224ULTRANS DISPOSABLE INTRAUTERINEK883832CATHETER, INTRAUTERINE AND INTRODUCER

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Related Devices (Code: HFN)

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.

K250897Koala Intrauterine Pressure Catheter (IPC-5000E)Clinical Innovations, LLCK974389KOALA INTRAUTERINE PRESSURE CATHETER, KOALA EXTERNAL INTRAUTERINE PRESSURE CATHETERClinical Innovations, Inc.K973746PRE-FILLED SYRINGE FOR KOALA IUPClinical Innovations, Inc.K961424INTRAN 500Utah Medical Products, Inc.K954955STORC INTRAUTERINE PRESSURE CATHETERClinical Innovations, Inc.K955443INTRAN PLUSUtah Medical Products, Inc.

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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