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FDA 510(k)

MULTI-CELL ULTRAFILTRATION SYSTEM

K-Number: K761100 · 1976-12-06

ApplicantAmicon, Inc.
Decision Date1976-12-06
Product CodeJQQ
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

MULTI-CELL ULTRAFILTRATION SYSTEM is the device name listed in this FDA 510(k) record. The listed applicant is Amicon, Inc.. It received FDA 510(k) clearance on 1976-12-06 under 510(k) number K761100. The device is classified under product code JQQ. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MULTI-CELL ULTRAFILTRATION SYSTEM?

MULTI-CELL ULTRAFILTRATION SYSTEM is a medical device that received FDA 510(k) clearance on 1976-12-06. The listed applicant is Amicon, Inc.. The 510(k) number is K761100.

When did MULTI-CELL ULTRAFILTRATION SYSTEM receive FDA 510(k) clearance?

MULTI-CELL ULTRAFILTRATION SYSTEM received FDA 510(k) clearance on 1976-12-06, under 510(k) number K761100.

Who is the listed applicant for MULTI-CELL ULTRAFILTRATION SYSTEM?

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

What is the FDA product code for MULTI-CELL ULTRAFILTRATION SYSTEM?

The FDA product code for MULTI-CELL ULTRAFILTRATION SYSTEM is JQQ.

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Other records listing Amicon, 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.

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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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