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FDA 510(k)

GARDOSI BIRTHING CUSHION

K-Number: K903973 · 1990-09-27

ApplicantGraphic Controls Corp.
Decision Date1990-09-27
Product CodeKNC
Advisory CommitteeOB
DecisionSubstantially Equivalent

Device Summary

GARDOSI BIRTHING CUSHION 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 1990-09-27 under 510(k) number K903973. 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 GARDOSI BIRTHING CUSHION?

GARDOSI BIRTHING CUSHION is a medical device that received FDA 510(k) clearance on 1990-09-27. The listed applicant is Graphic Controls Corp.. The 510(k) number is K903973.

When did GARDOSI BIRTHING CUSHION receive FDA 510(k) clearance?

GARDOSI BIRTHING CUSHION received FDA 510(k) clearance on 1990-09-27, under 510(k) number K903973.

Who is the listed applicant for GARDOSI BIRTHING CUSHION?

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 GARDOSI BIRTHING CUSHION?

The FDA product code for GARDOSI BIRTHING CUSHION is KNC.

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Other records listing Graphic Controls Corp. as applicant

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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.

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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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