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FDA 510(k)

MERIVAARA OBSTETRIC CHAIR/BED MODEL 358

K-Number: K852174 · 1985-09-06

Decision Date1985-09-06
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

MERIVAARA OBSTETRIC CHAIR/BED MODEL 358 is the device name listed in this FDA 510(k) record. The listed applicant is Daun International, Inc.. It received FDA 510(k) clearance on 1985-09-06 under 510(k) number K852174. The device is classified under product code KNC. It was reviewed by the OB advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVAARA OBSTETRIC CHAIR/BED MODEL 358?

MERIVAARA OBSTETRIC CHAIR/BED MODEL 358 is a medical device that received FDA 510(k) clearance on 1985-09-06. The listed applicant is Daun International, Inc.. The 510(k) number is K852174.

When did MERIVAARA OBSTETRIC CHAIR/BED MODEL 358 receive FDA 510(k) clearance?

MERIVAARA OBSTETRIC CHAIR/BED MODEL 358 received FDA 510(k) clearance on 1985-09-06, under 510(k) number K852174.

Who is the listed applicant for MERIVAARA OBSTETRIC CHAIR/BED MODEL 358?

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

What is the FDA product code for MERIVAARA OBSTETRIC CHAIR/BED MODEL 358?

The FDA product code for MERIVAARA OBSTETRIC CHAIR/BED MODEL 358 is KNC.

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 Daun International, 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 7 devices →

Related Devices (Code: KNC)

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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