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FDA 510(k)

ACUMED FLEXIBLE CANNULA

K-Number: K932099 · 1994-06-28

ApplicantAcu Med, Inc.
Decision Date1994-06-28
Product CodeHRX
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

ACUMED FLEXIBLE CANNULA is the device name listed in this FDA 510(k) record. The listed applicant is Acu Med, Inc.. It received FDA 510(k) clearance on 1994-06-28 under 510(k) number K932099. The device is classified under product code HRX. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACUMED FLEXIBLE CANNULA?

ACUMED FLEXIBLE CANNULA is a medical device that received FDA 510(k) clearance on 1994-06-28. The listed applicant is Acu Med, Inc.. The 510(k) number is K932099.

When did ACUMED FLEXIBLE CANNULA receive FDA 510(k) clearance?

ACUMED FLEXIBLE CANNULA received FDA 510(k) clearance on 1994-06-28, under 510(k) number K932099.

Who is the listed applicant for ACUMED FLEXIBLE CANNULA?

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

What is the FDA product code for ACUMED FLEXIBLE CANNULA?

The FDA product code for ACUMED FLEXIBLE CANNULA is HRX.

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Other records listing Acu Med, Inc. as applicant

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Related Devices (Code: HRX)

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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