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)

MERIVAARA EMERGENCY PATIENT TROLLEY #436

K-Number: K871556 · 1987-04-30

Decision Date1987-04-30
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MERIVAARA EMERGENCY PATIENT TROLLEY #436 is the device name listed in this FDA 510(k) record. The listed applicant is Global Medical Prods, Inc.. It received FDA 510(k) clearance on 1987-04-30 under 510(k) number K871556. The device is classified under product code FPO. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MERIVAARA EMERGENCY PATIENT TROLLEY #436?

MERIVAARA EMERGENCY PATIENT TROLLEY #436 is a medical device that received FDA 510(k) clearance on 1987-04-30. The listed applicant is Global Medical Prods, Inc.. The 510(k) number is K871556.

When did MERIVAARA EMERGENCY PATIENT TROLLEY #436 receive FDA 510(k) clearance?

MERIVAARA EMERGENCY PATIENT TROLLEY #436 received FDA 510(k) clearance on 1987-04-30, under 510(k) number K871556.

Who is the listed applicant for MERIVAARA EMERGENCY PATIENT TROLLEY #436?

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

What is the FDA product code for MERIVAARA EMERGENCY PATIENT TROLLEY #436?

The FDA product code for MERIVAARA EMERGENCY PATIENT TROLLEY #436 is FPO.

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 Global Medical Prods, Inc. 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 9 devices →

Related Devices (Code: FPO)

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.

↑