FDA 510(k)

BANANA KNIFE SERRATED

K-Number: K841973 · 1984-06-19

Decision Date1984-06-19

Product CodeHTZ

Advisory CommitteeSU

DecisionSubstantially Equivalent

Device Summary

BANANA KNIFE SERRATED is the device name listed in this FDA 510(k) record. The listed applicant is Stainless Mfg., Inc.. It received FDA 510(k) clearance on 1984-06-19 under 510(k) number K841973. The device is classified under product code HTZ. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANANA KNIFE SERRATED?

BANANA KNIFE SERRATED is a medical device that received FDA 510(k) clearance on 1984-06-19. The listed applicant is Stainless Mfg., Inc.. The 510(k) number is K841973.

When did BANANA KNIFE SERRATED receive FDA 510(k) clearance?

BANANA KNIFE SERRATED received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841973.

Who is the listed applicant for BANANA KNIFE SERRATED?

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

What is the FDA product code for BANANA KNIFE SERRATED?

The FDA product code for BANANA KNIFE SERRATED is HTZ.

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Other records listing Stainless Mfg., Inc. as applicant

K841980SIDE CUTTING SERRATED BLADE K8419775MM DOUGLE EDGE RING CURETTE K8419712.5MM & 4MM PROBE K841969-LABELING K841975ROSETTE KNIFE 4MM K841970CAMELBACK HANDLE-K841969-LABELING K8419814MM & 5MM FILE

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Related Devices (Code: HTZ)

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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.