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FDA 510(k)

TIP & MEMBRANE ASSEMBLY

K-Number: K921443 · 1993-06-22

ApplicantBio-Rad
Decision Date1993-06-22
Product CodeHKX
Advisory CommitteeOP
DecisionSubstantially Equivalent

Device Summary

TIP & MEMBRANE ASSEMBLY is the device name listed in this FDA 510(k) record. The listed applicant is Bio-Rad. It received FDA 510(k) clearance on 1993-06-22 under 510(k) number K921443. The device is classified under product code HKX. It was reviewed by the OP advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the TIP & MEMBRANE ASSEMBLY?

TIP & MEMBRANE ASSEMBLY is a medical device that received FDA 510(k) clearance on 1993-06-22. The listed applicant is Bio-Rad. The 510(k) number is K921443.

When did TIP & MEMBRANE ASSEMBLY receive FDA 510(k) clearance?

TIP & MEMBRANE ASSEMBLY received FDA 510(k) clearance on 1993-06-22, under 510(k) number K921443.

Who is the listed applicant for TIP & MEMBRANE ASSEMBLY?

The FDA 510(k) record lists Bio-Rad as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for TIP & MEMBRANE ASSEMBLY?

The FDA product code for TIP & MEMBRANE ASSEMBLY is HKX.

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Related Devices (Code: HKX)

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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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