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)

BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER

K-Number: K863083 · 1986-09-03

Decision Date1986-09-03
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER is the device name listed in this FDA 510(k) record. The listed applicant is Beta Medical Products Co.. It received FDA 510(k) clearance on 1986-09-03 under 510(k) number K863083. 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 BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER?

BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER is a medical device that received FDA 510(k) clearance on 1986-09-03. The listed applicant is Beta Medical Products Co.. The 510(k) number is K863083.

When did BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER receive FDA 510(k) clearance?

BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER received FDA 510(k) clearance on 1986-09-03, under 510(k) number K863083.

Who is the listed applicant for BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER?

The FDA 510(k) record lists Beta Medical Products Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER?

The FDA product code for BETA MEDICAL PRODUCTS EMR-301 HYDRAULIC STRETCHER 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 Beta Medical Products Co. 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: 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.

↑