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FDA 510(k)

RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY

K-Number: K870417 · 1987-03-05

ApplicantNorth Coast Medi-Tek
Decision Date1987-03-05
Product CodeFSM
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

RCT-1, RCT-2, RCT-3 ARTHROGRAM 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 1987-03-05 under 510(k) number K870417. The device is classified under product code FSM. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY?

RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY is a medical device that received FDA 510(k) clearance on 1987-03-05. The listed applicant is North Coast Medi-Tek. The 510(k) number is K870417.

When did RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY receive FDA 510(k) clearance?

RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY received FDA 510(k) clearance on 1987-03-05, under 510(k) number K870417.

Who is the listed applicant for RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY?

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

What is the FDA product code for RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY?

The FDA product code for RCT-1, RCT-2, RCT-3 ARTHROGRAM TRAY is FSM.

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.

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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.

K870419IVR-SP CUSTOM ANGIOGRAPHY TRAYK870420PTC-6 AND PTC-8 PERCUTANEOUS CHOLANGIOGRAPHYK870416LP EXTENSION SETSK870418MYA-1 AND MYT-1 MYELOGRAM TRAYK854095BIOPSY TRAY I & II

Related Devices (Code: FSM)

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.

K971217INSTRUMENT TRAY LINERGeneral Hospital Supply Corp.K962328SINGLE USE INSTRUMENT TRAYMedcare Medical Group, Inc.K944025SURGICAL INSTRUMENT TRAYRiley Medical, Inc.K912106ARTHROSCOPY TRAYMedical Device Inspection Co., Inc.K912053OPEN HEART TRAYMedical Device Inspection Co., Inc.K912052HEART CATH TRAYMedical Device Inspection Co., Inc.

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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