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FDA 510(k)

4MM CUP CURRETTE

K-Number: K841979 · 1984-06-19

ApplicantStainless Mfg., Inc.
Decision Date1984-06-19
Product CodeHTF
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

4MM CUP CURRETTE 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 K841979. The device is classified under product code HTF. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 4MM CUP CURRETTE?

4MM CUP CURRETTE 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 K841979.

When did 4MM CUP CURRETTE receive FDA 510(k) clearance?

4MM CUP CURRETTE received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841979.

Who is the listed applicant for 4MM CUP CURRETTE?

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 4MM CUP CURRETTE?

The FDA product code for 4MM CUP CURRETTE is HTF.

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Other records listing Stainless Mfg., 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.

K841980SIDE CUTTING SERRATED BLADEK8419775MM DOUGLE EDGE RING CURETTEK8419712.5MM & 4MM PROBE K841969-LABELINGK841975ROSETTE KNIFE 4MMK841970CAMELBACK HANDLE-K841969-LABELINGK8419814MM & 5MM FILE

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Related Devices (Code: HTF)

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.

K890252BONE CURETTEKinetic Medical ProductsK870778ACROMED WALLIE-HEINIG CURETTESBuckman Co., 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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