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FDA 510(k)

LASER PLUME FILTERS

K-Number: K862954 · 1986-08-14

ApplicantLifestream Int'L, Inc.
Decision Date1986-08-14
Product Code
DecisionSubstantially Equivalent

Device Summary

LASER PLUME FILTERS is the device name listed in this FDA 510(k) record. The listed applicant is Lifestream Int'L, Inc.. It received FDA 510(k) clearance on 1986-08-14 under 510(k) number K862954. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the LASER PLUME FILTERS?

LASER PLUME FILTERS is a medical device that received FDA 510(k) clearance on 1986-08-14. The listed applicant is Lifestream Int'L, Inc.. The 510(k) number is K862954.

When did LASER PLUME FILTERS receive FDA 510(k) clearance?

LASER PLUME FILTERS received FDA 510(k) clearance on 1986-08-14, under 510(k) number K862954.

Who is the listed applicant for LASER PLUME FILTERS?

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

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Other records listing Lifestream Int'L, 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.

K964571VISION CARDIOPLEGIA DELIVERY SYSTEMK962354DIOMED 15, 30, 60 SURGICAL DIODE LASERK920178CARDIOTOMY RESERVOIR W/20 MICRON FILITERK920618AUTOTRANSFUSION SUCTION SETK913181AUTOLOGOUS BLOOD PROCESSING SYSTEMK914396SURGI LIGHT NON-CONTACT FIBERS

View all 23 devices →

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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