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FDA 510(k)

BOOMERANG ABSORPTION COMENSATION FILTER

K-Number: K853330 · 1985-11-15

ApplicantEntreprises Octostop, Inc.
Decision Date1985-11-15
Product CodeKPR
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

BOOMERANG ABSORPTION COMENSATION FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Entreprises Octostop, Inc.. It received FDA 510(k) clearance on 1985-11-15 under 510(k) number K853330. The device is classified under product code KPR. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BOOMERANG ABSORPTION COMENSATION FILTER?

BOOMERANG ABSORPTION COMENSATION FILTER is a medical device that received FDA 510(k) clearance on 1985-11-15. The listed applicant is Entreprises Octostop, Inc.. The 510(k) number is K853330.

When did BOOMERANG ABSORPTION COMENSATION FILTER receive FDA 510(k) clearance?

BOOMERANG ABSORPTION COMENSATION FILTER received FDA 510(k) clearance on 1985-11-15, under 510(k) number K853330.

Who is the listed applicant for BOOMERANG ABSORPTION COMENSATION FILTER?

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

What is the FDA product code for BOOMERANG ABSORPTION COMENSATION FILTER?

The FDA product code for BOOMERANG ABSORPTION COMENSATION FILTER is KPR.

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Related Devices (Code: KPR)

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.

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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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