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)

INSTRUMENT CLEANING BRUSH

K-Number: K780399 · 1978-03-17

Decision Date1978-03-17
Product CodeKDC
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

INSTRUMENT CLEANING BRUSH is the device name listed in this FDA 510(k) record. The listed applicant is Ransom and Randolph. It received FDA 510(k) clearance on 1978-03-17 under 510(k) number K780399. The device is classified under product code KDC. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the INSTRUMENT CLEANING BRUSH?

INSTRUMENT CLEANING BRUSH is a medical device that received FDA 510(k) clearance on 1978-03-17. The listed applicant is Ransom and Randolph. The 510(k) number is K780399.

When did INSTRUMENT CLEANING BRUSH receive FDA 510(k) clearance?

INSTRUMENT CLEANING BRUSH received FDA 510(k) clearance on 1978-03-17, under 510(k) number K780399.

Who is the listed applicant for INSTRUMENT CLEANING BRUSH?

The FDA 510(k) record lists Ransom and Randolph as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for INSTRUMENT CLEANING BRUSH?

The FDA product code for INSTRUMENT CLEANING BRUSH is KDC.

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 Ransom and Randolph 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: KDC)

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.

↑