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FDA 510(k)

IMPLANTOLOGY MODULE, MODEL 2175

K-Number: K932492 · 1993-10-05

ApplicantMicro Surgical Instruments Corp.
Decision Date1993-10-05
Product CodeJEY
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

IMPLANTOLOGY MODULE, MODEL 2175 is the device name listed in this FDA 510(k) record. The listed applicant is Micro Surgical Instruments Corp.. It received FDA 510(k) clearance on 1993-10-05 under 510(k) number K932492. The device is classified under product code JEY. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the IMPLANTOLOGY MODULE, MODEL 2175?

IMPLANTOLOGY MODULE, MODEL 2175 is a medical device that received FDA 510(k) clearance on 1993-10-05. The listed applicant is Micro Surgical Instruments Corp.. The 510(k) number is K932492.

When did IMPLANTOLOGY MODULE, MODEL 2175 receive FDA 510(k) clearance?

IMPLANTOLOGY MODULE, MODEL 2175 received FDA 510(k) clearance on 1993-10-05, under 510(k) number K932492.

Who is the listed applicant for IMPLANTOLOGY MODULE, MODEL 2175?

The FDA 510(k) record lists Micro Surgical Instruments Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for IMPLANTOLOGY MODULE, MODEL 2175?

The FDA product code for IMPLANTOLOGY MODULE, MODEL 2175 is JEY.

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Related Devices (Code: JEY)

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.

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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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