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FDA 510(k)

MECONIUM SUCTION DEVICE (MSD)

K-Number: K914370 · 1993-01-06

Decision Date1993-01-06
Product CodeBTR
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

MECONIUM SUCTION DEVICE (MSD) is the device name listed in this FDA 510(k) record. The listed applicant is Vital Signs, Inc.. It received FDA 510(k) clearance on 1993-01-06 under 510(k) number K914370. The device is classified under product code BTR. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MECONIUM SUCTION DEVICE (MSD)?

MECONIUM SUCTION DEVICE (MSD) is a medical device that received FDA 510(k) clearance on 1993-01-06. The listed applicant is Vital Signs, Inc.. The 510(k) number is K914370.

When did MECONIUM SUCTION DEVICE (MSD) receive FDA 510(k) clearance?

MECONIUM SUCTION DEVICE (MSD) received FDA 510(k) clearance on 1993-01-06, under 510(k) number K914370.

Who is the listed applicant for MECONIUM SUCTION DEVICE (MSD)?

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

What is the FDA product code for MECONIUM SUCTION DEVICE (MSD)?

The FDA product code for MECONIUM SUCTION DEVICE (MSD) is BTR.

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 Vital Signs, 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 75 devices →

Related Devices (Code: BTR)

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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