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FDA 510(k)

BORRION ENTERPRISE CO

K-Number: K941340 · 1994-05-17

ApplicantBorrion Enterprise Co.
Decision Date1994-05-17
Product CodeHQY
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

BORRION ENTERPRISE CO is the device name listed in this FDA 510(k) record. The listed applicant is Borrion Enterprise Co.. It received FDA 510(k) clearance on 1994-05-17 under 510(k) number K941340. The device is classified under product code HQY. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BORRION ENTERPRISE CO?

BORRION ENTERPRISE CO is a medical device that received FDA 510(k) clearance on 1994-05-17. The listed applicant is Borrion Enterprise Co.. The 510(k) number is K941340.

When did BORRION ENTERPRISE CO receive FDA 510(k) clearance?

BORRION ENTERPRISE CO received FDA 510(k) clearance on 1994-05-17, under 510(k) number K941340.

Who is the listed applicant for BORRION ENTERPRISE CO?

The FDA 510(k) record lists Borrion Enterprise Co. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for BORRION ENTERPRISE CO?

The FDA product code for BORRION ENTERPRISE CO is HQY.

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Related Devices (Code: HQY)

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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