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FDA 510(k)

O.M.S. GUILLOTINE CUTTER

K-Number: K844374 · 1984-12-11

ApplicantOptical Micro Systems, Inc.
Decision Date1984-12-11
Product CodeHQE
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

O.M.S. GUILLOTINE CUTTER is the device name listed in this FDA 510(k) record. The listed applicant is Optical Micro Systems, Inc.. It received FDA 510(k) clearance on 1984-12-11 under 510(k) number K844374. The device is classified under product code HQE. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the O.M.S. GUILLOTINE CUTTER?

O.M.S. GUILLOTINE CUTTER is a medical device that received FDA 510(k) clearance on 1984-12-11. The listed applicant is Optical Micro Systems, Inc.. The 510(k) number is K844374.

When did O.M.S. GUILLOTINE CUTTER receive FDA 510(k) clearance?

O.M.S. GUILLOTINE CUTTER received FDA 510(k) clearance on 1984-12-11, under 510(k) number K844374.

Who is the listed applicant for O.M.S. GUILLOTINE CUTTER?

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

What is the FDA product code for O.M.S. GUILLOTINE CUTTER?

The FDA product code for O.M.S. GUILLOTINE CUTTER is HQE.

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Other records listing Optical Micro Systems, Inc. as applicant

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Related Devices (Code: HQE)

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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.

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