FDA 510(k)

J-CATHETER

K-Number: K820628 · 1982-04-06

Decision Date1982-04-06

Product Code

DecisionSubstantially Equivalent

Device Summary

J-CATHETER is the device name listed in this FDA 510(k) record. The listed applicant is Dna Medical, Inc.. It received FDA 510(k) clearance on 1982-04-06 under 510(k) number K820628. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the J-CATHETER?

J-CATHETER is a medical device that received FDA 510(k) clearance on 1982-04-06. The listed applicant is Dna Medical, Inc.. The 510(k) number is K820628.

When did J-CATHETER receive FDA 510(k) clearance?

J-CATHETER received FDA 510(k) clearance on 1982-04-06, under 510(k) number K820628.

Who is the listed applicant for J-CATHETER?

The FDA 510(k) record lists Dna Medical, Inc. 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.

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Other records listing Dna Medical, Inc. as applicant

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Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.