FDA 510(k)

KEYES SKIN PUNCH

K-Number: K854893 · 1985-12-24

Decision Date1985-12-24

Product Code

DecisionSubstantially Equivalent

Device Summary

KEYES SKIN PUNCH is the device name listed in this FDA 510(k) record. The listed applicant is Euro-Med Intl.. It received FDA 510(k) clearance on 1985-12-24 under 510(k) number K854893. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KEYES SKIN PUNCH?

KEYES SKIN PUNCH is a medical device that received FDA 510(k) clearance on 1985-12-24. The listed applicant is Euro-Med Intl.. The 510(k) number is K854893.

When did KEYES SKIN PUNCH receive FDA 510(k) clearance?

KEYES SKIN PUNCH received FDA 510(k) clearance on 1985-12-24, under 510(k) number K854893.

Who is the listed applicant for KEYES SKIN PUNCH?

The FDA 510(k) record lists Euro-Med Intl. as the applicant. This does not by itself establish the device manufacturer.

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Other records listing Euro-Med Intl. as applicant

K883884PROSTATIC CORE-CUT NEEDLE K882404KEVOR-CURETTE K854894SPOON K854890HOOK PROBE K854901PACIFIC GRASPER K854891KNIFE

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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.