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)

LIC MOBILE TRANSPORT STRETCHERS

K-Number: K861410 · 1986-04-22

Decision Date1986-04-22
Product CodeFPO
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

LIC MOBILE TRANSPORT STRETCHERS is the device name listed in this FDA 510(k) record. The listed applicant is Lada Intl., Inc.. It received FDA 510(k) clearance on 1986-04-22 under 510(k) number K861410. 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 LIC MOBILE TRANSPORT STRETCHERS?

LIC MOBILE TRANSPORT STRETCHERS is a medical device that received FDA 510(k) clearance on 1986-04-22. The listed applicant is Lada Intl., Inc.. The 510(k) number is K861410.

When did LIC MOBILE TRANSPORT STRETCHERS receive FDA 510(k) clearance?

LIC MOBILE TRANSPORT STRETCHERS received FDA 510(k) clearance on 1986-04-22, under 510(k) number K861410.

Who is the listed applicant for LIC MOBILE TRANSPORT STRETCHERS?

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

What is the FDA product code for LIC MOBILE TRANSPORT STRETCHERS?

The FDA product code for LIC MOBILE TRANSPORT STRETCHERS 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 Lada Intl., 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 7 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.

↑