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FDA 510(k)

COONS GASTROSTICK SYSTEM

K-Number: K852552 · 1985-10-17

ApplicantMedi-Tech, Inc.
Decision Date1985-10-17
Product CodeKNT
Advisory CommitteeGU
DecisionSubstantially Equivalent

Device Summary

COONS GASTROSTICK SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Medi-Tech, Inc.. It received FDA 510(k) clearance on 1985-10-17 under 510(k) number K852552. The device is classified under product code KNT. It was reviewed by the GU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COONS GASTROSTICK SYSTEM?

COONS GASTROSTICK SYSTEM is a medical device that received FDA 510(k) clearance on 1985-10-17. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K852552.

When did COONS GASTROSTICK SYSTEM receive FDA 510(k) clearance?

COONS GASTROSTICK SYSTEM received FDA 510(k) clearance on 1985-10-17, under 510(k) number K852552.

Who is the listed applicant for COONS GASTROSTICK SYSTEM?

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

What is the FDA product code for COONS GASTROSTICK SYSTEM?

The FDA product code for COONS GASTROSTICK SYSTEM is KNT.

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Other records listing Medi-Tech, Inc. as applicant

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Related Devices (Code: KNT)

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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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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