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FDA 510(k)

THE ULTIMATE

K-Number: K863665 · 1986-09-25

ApplicantMyocure, Inc.
Decision Date1986-09-25
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

THE ULTIMATE is the device name listed in this FDA 510(k) record. The listed applicant is Myocure, Inc.. It received FDA 510(k) clearance on 1986-09-25 under 510(k) number K863665. The device is classified under product code HNN. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the THE ULTIMATE?

THE ULTIMATE is a medical device that received FDA 510(k) clearance on 1986-09-25. The listed applicant is Myocure, Inc.. The 510(k) number is K863665.

When did THE ULTIMATE receive FDA 510(k) clearance?

THE ULTIMATE received FDA 510(k) clearance on 1986-09-25, under 510(k) number K863665.

Who is the listed applicant for THE ULTIMATE?

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

What is the FDA product code for THE ULTIMATE?

The FDA product code for THE ULTIMATE is HNN.

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 Myocure, 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.

K880346CANNULASK880347ANESTHESIA/RETROBULBAR NEEDLESK880345CYSTOTOMES/KNIFESK874057OPHTHALMIC TIP & BLADE SCALPELSK874056OPHTHALMIC DISPOSABLE BLADESK873385OPHTHALMIC PHACO-BLADE

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Related Devices (Code: HNN)

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.

K110166CLEARCUT S SAFETY KNIFEAlcon Research, Ltd.K922378OPHTHALMIC KNIFEMicroptics Development LaboratoryK882402RETRACTIVE INCISION MICROMETER (RIM) GUAGEOptical CenterK881669MVR/STILETTO BLADE 20GA. - P/N 1900Advanced Surgical Products, Inc.K874979PRISMA DISPOSABLE MVR/STILETTO BLADEAdvanced Surgical Products, Inc.K874057OPHTHALMIC TIP & BLADE SCALPELSMyocure, Inc.

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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