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)

GLOVES, FLOOR

K-Number: K780181 · 1978-02-21

Decision Date1978-02-21
Product CodeFML
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

GLOVES, FLOOR is the device name listed in this FDA 510(k) record. The listed applicant is Tillotson Rubber Co., Inc.. It received FDA 510(k) clearance on 1978-02-21 under 510(k) number K780181. The device is classified under product code FML. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the GLOVES, FLOOR?

GLOVES, FLOOR is a medical device that received FDA 510(k) clearance on 1978-02-21. The listed applicant is Tillotson Rubber Co., Inc.. The 510(k) number is K780181.

When did GLOVES, FLOOR receive FDA 510(k) clearance?

GLOVES, FLOOR received FDA 510(k) clearance on 1978-02-21, under 510(k) number K780181.

Who is the listed applicant for GLOVES, FLOOR?

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

What is the FDA product code for GLOVES, FLOOR?

The FDA product code for GLOVES, FLOOR is FML.

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 Tillotson Rubber Co., 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.

Related Devices (Code: FML)

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.

↑