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FDA 510(k)

CUTTER JET

K-Number: K801651 · 1980-08-13

ApplicantCutter Laboratories, Inc.
Decision Date1980-08-13
Product CodeEFB
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

CUTTER JET is the device name listed in this FDA 510(k) record. The listed applicant is Cutter Laboratories, Inc.. It received FDA 510(k) clearance on 1980-08-13 under 510(k) number K801651. The device is classified under product code EFB. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CUTTER JET?

CUTTER JET is a medical device that received FDA 510(k) clearance on 1980-08-13. The listed applicant is Cutter Laboratories, Inc.. The 510(k) number is K801651.

When did CUTTER JET receive FDA 510(k) clearance?

CUTTER JET received FDA 510(k) clearance on 1980-08-13, under 510(k) number K801651.

Who is the listed applicant for CUTTER JET?

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

What is the FDA product code for CUTTER JET?

The FDA product code for CUTTER JET is EFB.

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Other records listing Cutter Laboratories, Inc. as applicant

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Related Devices (Code: EFB)

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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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