Disclaimer: This site aggregates publicly available data from official government sources (FDA, ClinicalTrials.gov, PubMed, SEC EDGAR) for general reference only. It does NOT constitute medical advice, diagnosis, treatment recommendations, or investment advice.

FDA 510(k)

Automatic Tissue Processing Unit

K-Number: K172717 · 2018-05-25

ApplicantBsl Co.
Decision Date2018-05-25
Product CodeMUU
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

Automatic Tissue Processing Unit is the device name listed in this FDA 510(k) record. The listed applicant is Bsl Co.. It received FDA 510(k) clearance on 2018-05-25 under 510(k) number K172717. The device is classified under product code MUU. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the Automatic Tissue Processing Unit?

Automatic Tissue Processing Unit is a medical device that received FDA 510(k) clearance on 2018-05-25. The listed applicant is Bsl Co.. The 510(k) number is K172717.

When did Automatic Tissue Processing Unit receive FDA 510(k) clearance?

Automatic Tissue Processing Unit received FDA 510(k) clearance on 2018-05-25, under 510(k) number K172717.

Who is the listed applicant for Automatic Tissue Processing Unit?

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

What is the FDA product code for Automatic Tissue Processing Unit?

The FDA product code for Automatic Tissue Processing Unit is MUU.

Other records listing Bsl Co. 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.

K202443Smart Kit Basic, Smart Kit Pro

Related Devices (Code: MUU)

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.

K210528IntelliFat Disposable Adipose Tissue Harvesting and Transfer Kit, IntelliFat Body On Demand (BOD) KitMillennium Medical Technologies Inc (Dba Cellmyx)K203800SyntrFuge SystemSyntr Health Technologies, Inc.K202443Smart Kit Basic, Smart Kit ProBsl Co., Ltd.K193539REVOLVE ENVI 600 Advanced Adipose SystemLifecell CorporationK193363Dermapose RefreshPuregraft, LLCK182732JTL-250-01Jointechlabs, Inc.

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.

↑