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FDA 510(k)

CARBOL-FUCHSIN, ZIEHL-NEEDSEN

K-Number: K842933 · 1984-09-11

Decision Date1984-09-11
Product CodeICL
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

CARBOL-FUCHSIN, ZIEHL-NEEDSEN is the device name listed in this FDA 510(k) record. The listed applicant is E K Ind., Inc.. It received FDA 510(k) clearance on 1984-09-11 under 510(k) number K842933. The device is classified under product code ICL. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBOL-FUCHSIN, ZIEHL-NEEDSEN?

CARBOL-FUCHSIN, ZIEHL-NEEDSEN is a medical device that received FDA 510(k) clearance on 1984-09-11. The listed applicant is E K Ind., Inc.. The 510(k) number is K842933.

When did CARBOL-FUCHSIN, ZIEHL-NEEDSEN receive FDA 510(k) clearance?

CARBOL-FUCHSIN, ZIEHL-NEEDSEN received FDA 510(k) clearance on 1984-09-11, under 510(k) number K842933.

Who is the listed applicant for CARBOL-FUCHSIN, ZIEHL-NEEDSEN?

The FDA 510(k) record lists E K Ind., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for CARBOL-FUCHSIN, ZIEHL-NEEDSEN?

The FDA product code for CARBOL-FUCHSIN, ZIEHL-NEEDSEN is ICL.

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 E K Ind., Inc. 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.

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Related Devices (Code: ICL)

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

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

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