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FDA 510(k)

MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE

K-Number: K844553 · 1984-12-11

ApplicantCodman & Shurtleff, Inc.
Decision Date1984-12-11
Product CodeHNN
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE is the device name listed in this FDA 510(k) record. The listed applicant is Codman & Shurtleff, Inc.. It received FDA 510(k) clearance on 1984-12-11 under 510(k) number K844553. 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 MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE?

MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE is a medical device that received FDA 510(k) clearance on 1984-12-11. The listed applicant is Codman & Shurtleff, Inc.. The 510(k) number is K844553.

When did MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE receive FDA 510(k) clearance?

MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE received FDA 510(k) clearance on 1984-12-11, under 510(k) number K844553.

Who is the listed applicant for MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE?

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

What is the FDA product code for MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE?

The FDA product code for MICRA DIAMOND KNIFE MICRA ADJUSTABLE KNIFE is HNN.

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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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