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FDA 510(k)

MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.

K-Number: K882080 · 1989-03-01

ApplicantAequitron Medical, Inc.
Decision Date1989-03-01
Product CodeHFM
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS. is the device name listed in this FDA 510(k) record. The listed applicant is Aequitron Medical, Inc.. It received FDA 510(k) clearance on 1989-03-01 under 510(k) number K882080. The device is classified under product code HFM. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.?

MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS. is a medical device that received FDA 510(k) clearance on 1989-03-01. The listed applicant is Aequitron Medical, Inc.. The 510(k) number is K882080.

When did MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS. receive FDA 510(k) clearance?

MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS. received FDA 510(k) clearance on 1989-03-01, under 510(k) number K882080.

Who is the listed applicant for MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.?

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

What is the FDA product code for MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS.?

The FDA product code for MODEL NUMBER (TBD) TOCO DATA TELEPHONE TRANS. SYS. is HFM.

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Other records listing Aequitron Medical, 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.

K961972MODEL AMI INFANT CENTRAL APHEA/HEART RATE MONITORK952880MODEL LP-1000 VOLUME VENTILATORK944654OXYGEN CONCENTRATION INDICATORK914424MODEL 6213 REMOTE ALARMK915381PORTABLE OXYGEN GENERATORK911399NASAL CPAP (CONTINUOUS POSITIVE AIR PRESSURE SYST)

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Related Devices (Code: HFM)

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.

K061044FEATHERLITE AQUA TOCODYNAMOMETERVentrex, Inc.K040392TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORINGAmerican I.V. Products, Inc.K013477TOCO LITE, MODEL TD-01Ventrex, Inc.K994353SECURELINE DISPOSABLE FETAL MONITORING STRAPS #3860 AND #3565Precision Dynamics Corp.K992811TRANSDUCERS FOR ULTRASOUND AND TOCODYNAMOMETER FETAL MONITORINGEpic Medical Equipment Services, Inc.K954847DISCO UTERINE CONTRACTION TRANSDUCER & ACCESSORIESOcg Systems, 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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