FDA 510(k)

THE SAVER KIT

K-Number: K863666 · 1986-10-20

Decision Date1986-10-20

Product Code

DecisionSubstantially Equivalent

Device Summary

THE SAVER KIT is the device name listed in this FDA 510(k) record. The listed applicant is Myocure, Inc.. It received FDA 510(k) clearance on 1986-10-20 under 510(k) number K863666. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE SAVER KIT?

THE SAVER KIT is a medical device that received FDA 510(k) clearance on 1986-10-20. The listed applicant is Myocure, Inc.. The 510(k) number is K863666.

When did THE SAVER KIT receive FDA 510(k) clearance?

THE SAVER KIT received FDA 510(k) clearance on 1986-10-20, under 510(k) number K863666.

Who is the listed applicant for THE SAVER KIT?

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

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Other records listing Myocure, Inc. as applicant

K880345CYSTOTOMES/KNIFES K880347ANESTHESIA/RETROBULBAR NEEDLES K880346CANNULAS K874057OPHTHALMIC TIP & BLADE SCALPELS K874056OPHTHALMIC DISPOSABLE BLADES K873385OPHTHALMIC PHACO-BLADE

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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.