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FDA 510(k)

FETAL MONITORING SPIRAL ELECTRODE

K-Number: K905130 · 1991-01-29

Decision Date1991-01-29
Product CodeHGP
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

FETAL MONITORING SPIRAL ELECTRODE is the device name listed in this FDA 510(k) record. The listed applicant is Graphic Controls Corp.. It received FDA 510(k) clearance on 1991-01-29 under 510(k) number K905130. The device is classified under product code HGP. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FETAL MONITORING SPIRAL ELECTRODE?

FETAL MONITORING SPIRAL ELECTRODE is a medical device that received FDA 510(k) clearance on 1991-01-29. The listed applicant is Graphic Controls Corp.. The 510(k) number is K905130.

When did FETAL MONITORING SPIRAL ELECTRODE receive FDA 510(k) clearance?

FETAL MONITORING SPIRAL ELECTRODE received FDA 510(k) clearance on 1991-01-29, under 510(k) number K905130.

Who is the listed applicant for FETAL MONITORING SPIRAL ELECTRODE?

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

What is the FDA product code for FETAL MONITORING SPIRAL ELECTRODE?

The FDA product code for FETAL MONITORING SPIRAL ELECTRODE is HGP.

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 Graphic Controls 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.

View all 55 devices →

Related Devices (Code: HGP)

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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