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FDA 510(k)

CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000

K-Number: K862509 · 1986-07-23

ApplicantLifestream Int'L, Inc.
Decision Date1986-07-23
Product CodeJDY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000 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 1986-07-23 under 510(k) number K862509. The device is classified under product code JDY. It was reviewed by the OR advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000?

CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000 is a medical device that received FDA 510(k) clearance on 1986-07-23. The listed applicant is Lifestream Int'L, Inc.. The 510(k) number is K862509.

When did CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000 receive FDA 510(k) clearance?

CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000 received FDA 510(k) clearance on 1986-07-23, under 510(k) number K862509.

Who is the listed applicant for CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000?

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

What is the FDA product code for CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000?

The FDA product code for CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000 is JDY.

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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

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Related Devices (Code: JDY)

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.

K902167CONTAIN(TM) LASER PLUME FILTERArbor Technologies, Inc.K902056LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTERHollister, Inc.K810542CEMENT FUME EVACUATOR TANK & FILTERWalgen Medical InnoventionsK790877BIOVAC: LFA LASER FUME (SMOKE) EVACUATIOStackhouse Assoc.K780202MONOMER EVACUATION SYSTEMMedishield, Inc.K770690MASK, VAPOR, MONOMERHowmedica Corp.

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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