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FDA 510(k)

2.5MM & 4MM PROBE K841969-LABELING

K-Number: K841971 · 1984-06-19

ApplicantStainless Mfg., Inc.
Decision Date1984-06-19
Product CodeHXB
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

2.5MM & 4MM PROBE K841969-LABELING 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 K841971. The device is classified under product code HXB. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the 2.5MM & 4MM PROBE K841969-LABELING?

2.5MM & 4MM PROBE K841969-LABELING 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 K841971.

When did 2.5MM & 4MM PROBE K841969-LABELING receive FDA 510(k) clearance?

2.5MM & 4MM PROBE K841969-LABELING received FDA 510(k) clearance on 1984-06-19, under 510(k) number K841971.

Who is the listed applicant for 2.5MM & 4MM PROBE K841969-LABELING?

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 2.5MM & 4MM PROBE K841969-LABELING?

The FDA product code for 2.5MM & 4MM PROBE K841969-LABELING is HXB.

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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 BLADEK8419814MM & 5MM FILEK841975ROSETTE KNIFE 4MMK841970CAMELBACK HANDLE-K841969-LABELINGK8419775MM DOUGLE EDGE RING CURETTEK841974RETROGRADE KNIFE 4MM & 5MM

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Related Devices (Code: HXB)

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.

K960539DIAO HAND SURGERY SETKinetikos Medical, Inc.K943472COHORT AVB RETRACTOR SYSTEMCohort Medical Products Group, Inc.K912843FLEXMEDICS RETRACT ORTH PROBE, PETTINE BONE PROBEFlexmedicsK890227SURGICAL PROBEKinetic Medical ProductsK873651BLUNT MEASURING PROBE W/2MM GRADATIONS #TM-1375Arthropedics, Inc.K873652HOOK PROBE #TM-1376Arthropedics, 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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