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FDA 510(k)

MEND APC

K-Number: K924094 · 1993-03-30

ApplicantMend Technologies, Inc.
Decision Date1993-03-30
Product CodeJEA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

MEND APC is the device name listed in this FDA 510(k) record. The listed applicant is Mend Technologies, Inc.. It received FDA 510(k) clearance on 1993-03-30 under 510(k) number K924094. The device is classified under product code JEA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MEND APC?

MEND APC is a medical device that received FDA 510(k) clearance on 1993-03-30. The listed applicant is Mend Technologies, Inc.. The 510(k) number is K924094.

When did MEND APC receive FDA 510(k) clearance?

MEND APC received FDA 510(k) clearance on 1993-03-30, under 510(k) number K924094.

Who is the listed applicant for MEND APC?

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

What is the FDA product code for MEND APC?

The FDA product code for MEND APC is JEA.

Other records listing Mend Technologies, 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.

K883867CERVICAL BIOPSY INSTRUMENTK884558IOP ADJUSTABLE STIRRUP

Related Devices (Code: JEA)

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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