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FDA 510(k)

MODEL 500 PEDIATRIC STRETCHER/CRIB

K-Number: K852422 · 1985-07-05

ApplicantMidmark Corp.
Decision Date1985-07-05
Product CodeFMS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MODEL 500 PEDIATRIC STRETCHER/CRIB is the device name listed in this FDA 510(k) record. The listed applicant is Midmark Corp.. It received FDA 510(k) clearance on 1985-07-05 under 510(k) number K852422. 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 MODEL 500 PEDIATRIC STRETCHER/CRIB?

MODEL 500 PEDIATRIC STRETCHER/CRIB is a medical device that received FDA 510(k) clearance on 1985-07-05. The listed applicant is Midmark Corp.. The 510(k) number is K852422.

When did MODEL 500 PEDIATRIC STRETCHER/CRIB receive FDA 510(k) clearance?

MODEL 500 PEDIATRIC STRETCHER/CRIB received FDA 510(k) clearance on 1985-07-05, under 510(k) number K852422.

Who is the listed applicant for MODEL 500 PEDIATRIC STRETCHER/CRIB?

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

What is the FDA product code for MODEL 500 PEDIATRIC STRETCHER/CRIB?

The FDA product code for MODEL 500 PEDIATRIC STRETCHER/CRIB 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.

Other records listing Midmark Corp. 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 31 devices →

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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