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FDA 510(k)

FILTER SAMPLER BLOOD SERUM FILTER

K-Number: K771985 · 1977-11-02

ApplicantClasrock
Decision Date1977-11-02
Product CodeGIM
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

FILTER SAMPLER BLOOD SERUM FILTER is the device name listed in this FDA 510(k) record. The listed applicant is Clasrock. It received FDA 510(k) clearance on 1977-11-02 under 510(k) number K771985. The device is classified under product code GIM. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the FILTER SAMPLER BLOOD SERUM FILTER?

FILTER SAMPLER BLOOD SERUM FILTER is a medical device that received FDA 510(k) clearance on 1977-11-02. The listed applicant is Clasrock. The 510(k) number is K771985.

When did FILTER SAMPLER BLOOD SERUM FILTER receive FDA 510(k) clearance?

FILTER SAMPLER BLOOD SERUM FILTER received FDA 510(k) clearance on 1977-11-02, under 510(k) number K771985.

Who is the listed applicant for FILTER SAMPLER BLOOD SERUM FILTER?

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

What is the FDA product code for FILTER SAMPLER BLOOD SERUM FILTER?

The FDA product code for FILTER SAMPLER BLOOD SERUM FILTER is GIM.

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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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