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)

MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL

K-Number: K890855 · 1989-05-01

Decision Date1989-05-01
Product CodeLNH
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL is the device name listed in this FDA 510(k) record. The listed applicant is Medical Advances, Inc.. It received FDA 510(k) clearance on 1989-05-01 under 510(k) number K890855. The device is classified under product code LNH. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL?

MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL is a medical device that received FDA 510(k) clearance on 1989-05-01. The listed applicant is Medical Advances, Inc.. The 510(k) number is K890855.

When did MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL receive FDA 510(k) clearance?

MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL received FDA 510(k) clearance on 1989-05-01, under 510(k) number K890855.

Who is the listed applicant for MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL?

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

What is the FDA product code for MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL?

The FDA product code for MODEL 4041; 4 ANGLED PAIR CRC SURFACE COIL is LNH.

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 Medical Advances, 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 57 devices →

Related Devices (Code: LNH)

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.

↑