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FDA 510(k)

CENTURY BIRTHING CHAIR

K-Number: K811902 · 1981-08-25

Decision Date1981-08-25
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

CENTURY BIRTHING CHAIR is the device name listed in this FDA 510(k) record. The listed applicant is Century Manufacturing Co.. It received FDA 510(k) clearance on 1981-08-25 under 510(k) number K811902. 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 CENTURY BIRTHING CHAIR?

CENTURY BIRTHING CHAIR is a medical device that received FDA 510(k) clearance on 1981-08-25. The listed applicant is Century Manufacturing Co.. The 510(k) number is K811902.

When did CENTURY BIRTHING CHAIR receive FDA 510(k) clearance?

CENTURY BIRTHING CHAIR received FDA 510(k) clearance on 1981-08-25, under 510(k) number K811902.

Who is the listed applicant for CENTURY BIRTHING CHAIR?

The FDA 510(k) record lists Century Manufacturing Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CENTURY BIRTHING CHAIR?

The FDA product code for CENTURY BIRTHING CHAIR 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 Century Manufacturing Co. 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 12 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

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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