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FDA 510(k)

BIO-CSF LIQUID CONTROL LEVEL 1 AND 2

K-Number: K963551 · 1996-10-07

Decision Date1996-10-07
Product CodeJJX
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 is the device name listed in this FDA 510(k) record. The listed applicant is Biocell Laboratories, Inc.. It received FDA 510(k) clearance on 1996-10-07 under 510(k) number K963551. The device is classified under product code JJX. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIO-CSF LIQUID CONTROL LEVEL 1 AND 2?

BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 is a medical device that received FDA 510(k) clearance on 1996-10-07. The listed applicant is Biocell Laboratories, Inc.. The 510(k) number is K963551.

When did BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 receive FDA 510(k) clearance?

BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 received FDA 510(k) clearance on 1996-10-07, under 510(k) number K963551.

Who is the listed applicant for BIO-CSF LIQUID CONTROL LEVEL 1 AND 2?

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

What is the FDA product code for BIO-CSF LIQUID CONTROL LEVEL 1 AND 2?

The FDA product code for BIO-CSF LIQUID CONTROL LEVEL 1 AND 2 is JJX.

Related Clinical Trials

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.

Other records listing Biocell Laboratories, 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.

Related Devices (Code: JJX)

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.

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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