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FDA 510(k)

OBTRASOUND STETHOSCOPE FETAL CALC

K-Number: K911453 · 1991-06-20

Decision Date1991-06-20
Product CodeKNG
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

OBTRASOUND STETHOSCOPE FETAL CALC is the device name listed in this FDA 510(k) record. The listed applicant is Medasonics, Inc.. It received FDA 510(k) clearance on 1991-06-20 under 510(k) number K911453. The device is classified under product code KNG. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the OBTRASOUND STETHOSCOPE FETAL CALC?

OBTRASOUND STETHOSCOPE FETAL CALC is a medical device that received FDA 510(k) clearance on 1991-06-20. The listed applicant is Medasonics, Inc.. The 510(k) number is K911453.

When did OBTRASOUND STETHOSCOPE FETAL CALC receive FDA 510(k) clearance?

OBTRASOUND STETHOSCOPE FETAL CALC received FDA 510(k) clearance on 1991-06-20, under 510(k) number K911453.

Who is the listed applicant for OBTRASOUND STETHOSCOPE FETAL CALC?

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

What is the FDA product code for OBTRASOUND STETHOSCOPE FETAL CALC?

The FDA product code for OBTRASOUND STETHOSCOPE FETAL CALC is KNG.

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 Medasonics, 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 19 devices →

Related Devices (Code: KNG)

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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