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FDA 510(k)

MYA-1 AND MYT-1 MYELOGRAM TRAY

K-Number: K870418 · 1987-03-17

Decision Date1987-03-17
Product Code
DecisionSubstantially Equivalent

Device Summary

MYA-1 AND MYT-1 MYELOGRAM TRAY is the device name listed in this FDA 510(k) record. The listed applicant is North Coast Medi-Tek. It received FDA 510(k) clearance on 1987-03-17 under 510(k) number K870418. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MYA-1 AND MYT-1 MYELOGRAM TRAY?

MYA-1 AND MYT-1 MYELOGRAM TRAY is a medical device that received FDA 510(k) clearance on 1987-03-17. The listed applicant is North Coast Medi-Tek. The 510(k) number is K870418.

When did MYA-1 AND MYT-1 MYELOGRAM TRAY receive FDA 510(k) clearance?

MYA-1 AND MYT-1 MYELOGRAM TRAY received FDA 510(k) clearance on 1987-03-17, under 510(k) number K870418.

Who is the listed applicant for MYA-1 AND MYT-1 MYELOGRAM TRAY?

The FDA 510(k) record lists North Coast Medi-Tek as the applicant. This does not by itself establish the device manufacturer.

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 North Coast Medi-Tek 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.

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.

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