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FDA 510(k)

PREP SET CAT.#908

K-Number: K802020 · 1980-09-09

ApplicantPollak (Intl.), Ltd.
Decision Date1980-09-09
Product CodeKXF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

PREP SET CAT.#908 is the device name listed in this FDA 510(k) record. The listed applicant is Pollak (Intl.), Ltd.. It received FDA 510(k) clearance on 1980-09-09 under 510(k) number K802020. The device is classified under product code KXF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PREP SET CAT.#908?

PREP SET CAT.#908 is a medical device that received FDA 510(k) clearance on 1980-09-09. The listed applicant is Pollak (Intl.), Ltd.. The 510(k) number is K802020.

When did PREP SET CAT.#908 receive FDA 510(k) clearance?

PREP SET CAT.#908 received FDA 510(k) clearance on 1980-09-09, under 510(k) number K802020.

Who is the listed applicant for PREP SET CAT.#908?

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

What is the FDA product code for PREP SET CAT.#908?

The FDA product code for PREP SET CAT.#908 is KXF.

Other records listing Pollak (Intl.), Ltd. 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.

K000227UMBICUTK810049PEDICAT*K810050VECAFIX*K802011INFUSSION ALARM SYSTEM I.A.S. CAT.#1118K802009FLOWCLAMP CAT.#1011 & 1012K802017DRESSING CHANGE SET CAT.#910-930

View all 31 devices →

Related Devices (Code: KXF)

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.

K123184FINN CHAMBERS AQUASmartpracticeK103409ALLERGEAZE R CLEARSmartpracticeK063160ALLERGEAZE PATCH TEST CHAMBERSSmartpracticeK013820FINN CHAMBER (R)Epitest Ltd. OYK992553IQ CHAMBERSDormer Laboratories, Inc.K870762EAR APPLICATOR, CATALOG NO. 2229Treace Medical, 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.

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