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)

COLIN ELECTRONICS CO., LTD. STBP 680

K-Number: K854481 · 1986-06-09

Decision Date1986-06-09
Product CodeDXN
Advisory CommitteeCV
DecisionSubstantially Equivalent

Device Summary

COLIN ELECTRONICS CO., LTD. STBP 680 is the device name listed in this FDA 510(k) record. The listed applicant is Colin Medical Instruments Corp.. It received FDA 510(k) clearance on 1986-06-09 under 510(k) number K854481. The device is classified under product code DXN. It was reviewed by the CV advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COLIN ELECTRONICS CO., LTD. STBP 680?

COLIN ELECTRONICS CO., LTD. STBP 680 is a medical device that received FDA 510(k) clearance on 1986-06-09. The listed applicant is Colin Medical Instruments Corp.. The 510(k) number is K854481.

When did COLIN ELECTRONICS CO., LTD. STBP 680 receive FDA 510(k) clearance?

COLIN ELECTRONICS CO., LTD. STBP 680 received FDA 510(k) clearance on 1986-06-09, under 510(k) number K854481.

Who is the listed applicant for COLIN ELECTRONICS CO., LTD. STBP 680?

The FDA 510(k) record lists Colin Medical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COLIN ELECTRONICS CO., LTD. STBP 680?

The FDA product code for COLIN ELECTRONICS CO., LTD. STBP 680 is DXN.

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 Colin Medical Instruments Corp. 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 15 devices →

Related Devices (Code: DXN)

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.

↑