Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

CRIB CUDDLE - INFANT BED

K-Number: K845004 · 1986-04-23

Decision Date1986-04-23
Product CodeFMS
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

CRIB CUDDLE - INFANT BED is the device name listed in this FDA 510(k) record. The listed applicant is International Purchasing Services. It received FDA 510(k) clearance on 1986-04-23 under 510(k) number K845004. 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 CRIB CUDDLE - INFANT BED?

CRIB CUDDLE - INFANT BED is a medical device that received FDA 510(k) clearance on 1986-04-23. The listed applicant is International Purchasing Services. The 510(k) number is K845004.

When did CRIB CUDDLE - INFANT BED receive FDA 510(k) clearance?

CRIB CUDDLE - INFANT BED received FDA 510(k) clearance on 1986-04-23, under 510(k) number K845004.

Who is the listed applicant for CRIB CUDDLE - INFANT BED?

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

What is the FDA product code for CRIB CUDDLE - INFANT BED?

The FDA product code for CRIB CUDDLE - INFANT BED 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 International Purchasing Services 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.

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

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

↑