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FDA 510(k)

LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER

K-Number: K902056 · 1990-10-30

ApplicantHollister, Inc.
Decision Date1990-10-30
Product CodeJDY
Advisory CommitteeOR
DecisionSubstantially Equivalent

Device Summary

LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Hollister, Inc.. It received FDA 510(k) clearance on 1990-10-30 under 510(k) number K902056. 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 LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER?

LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER is a medical device that received FDA 510(k) clearance on 1990-10-30. The listed applicant is Hollister, Inc.. The 510(k) number is K902056.

When did LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER receive FDA 510(k) clearance?

LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER received FDA 510(k) clearance on 1990-10-30, under 510(k) number K902056.

Who is the listed applicant for LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER?

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

What is the FDA product code for LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER?

The FDA product code for LASER TRAP 100 LASER PLUME SMOKE EVACUATION FILTER is JDY.

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Other records listing Hollister, Inc. as applicant

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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.K862509CHARCOAL LASER SMOKE FILTER CATALOG NO. 901103-000Lifestream Int'L, 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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