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)

PAD, PRE-OPERATIVE PREPARATION

K-Number: K850811 · 1985-03-21

Decision Date1985-03-21
Product CodeKME
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PAD, PRE-OPERATIVE PREPARATION is the device name listed in this FDA 510(k) record. The listed applicant is East Texas Lighthouse For the Blind. It received FDA 510(k) clearance on 1985-03-21 under 510(k) number K850811. The device is classified under product code KME. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAD, PRE-OPERATIVE PREPARATION?

PAD, PRE-OPERATIVE PREPARATION is a medical device that received FDA 510(k) clearance on 1985-03-21. The listed applicant is East Texas Lighthouse For the Blind. The 510(k) number is K850811.

When did PAD, PRE-OPERATIVE PREPARATION receive FDA 510(k) clearance?

PAD, PRE-OPERATIVE PREPARATION received FDA 510(k) clearance on 1985-03-21, under 510(k) number K850811.

Who is the listed applicant for PAD, PRE-OPERATIVE PREPARATION?

The FDA 510(k) record lists East Texas Lighthouse For the Blind as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAD, PRE-OPERATIVE PREPARATION?

The FDA product code for PAD, PRE-OPERATIVE PREPARATION is KME.

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 East Texas Lighthouse For the Blind 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: KME)

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.

↑