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FDA 510(k)

N.K. PEDIATRIC CRIBS

K-Number: K853355 · 1985-09-20

Decision Date1985-09-20
Product CodeFMS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

N.K. PEDIATRIC CRIBS is the device name listed in this FDA 510(k) record. The listed applicant is N.K. Medical Products, Inc.. It received FDA 510(k) clearance on 1985-09-20 under 510(k) number K853355. The device is classified under product code FMS. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the N.K. PEDIATRIC CRIBS?

N.K. PEDIATRIC CRIBS is a medical device that received FDA 510(k) clearance on 1985-09-20. The listed applicant is N.K. Medical Products, Inc.. The 510(k) number is K853355.

When did N.K. PEDIATRIC CRIBS receive FDA 510(k) clearance?

N.K. PEDIATRIC CRIBS received FDA 510(k) clearance on 1985-09-20, under 510(k) number K853355.

Who is the listed applicant for N.K. PEDIATRIC CRIBS?

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

What is the FDA product code for N.K. PEDIATRIC CRIBS?

The FDA product code for N.K. PEDIATRIC CRIBS is FMS.

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.

Related Devices (Code: FMS)

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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