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FDA 510(k)

MEDI-TECH DILATATION CATHETERS

K-Number: K844292 · 1984-11-23

ApplicantMedi-Tech, Inc.
Decision Date1984-11-23
Product CodeLCN
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

MEDI-TECH DILATATION CATHETERS 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 1984-11-23 under 510(k) number K844292. The device is classified under product code LCN. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEDI-TECH DILATATION CATHETERS?

MEDI-TECH DILATATION CATHETERS is a medical device that received FDA 510(k) clearance on 1984-11-23. The listed applicant is Medi-Tech, Inc.. The 510(k) number is K844292.

When did MEDI-TECH DILATATION CATHETERS receive FDA 510(k) clearance?

MEDI-TECH DILATATION CATHETERS received FDA 510(k) clearance on 1984-11-23, under 510(k) number K844292.

Who is the listed applicant for MEDI-TECH DILATATION CATHETERS?

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 MEDI-TECH DILATATION CATHETERS?

The FDA product code for MEDI-TECH DILATATION CATHETERS is LCN.

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Other records listing Medi-Tech, Inc. as applicant

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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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