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FDA 510(k)

FILTER SAMPLER BLOOD SERUM FILTER

K-Number: K811036 · 1981-04-29

ApplicantGlasrock Plastics, Inc.
Decision Date1981-04-29
Product CodeJKA
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 Glasrock Plastics, Inc.. It received FDA 510(k) clearance on 1981-04-29 under 510(k) number K811036. The device is classified under product code JKA. 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 1981-04-29. The listed applicant is Glasrock Plastics, Inc.. The 510(k) number is K811036.

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

FILTER SAMPLER BLOOD SERUM FILTER received FDA 510(k) clearance on 1981-04-29, under 510(k) number K811036.

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

The FDA 510(k) record lists Glasrock Plastics, Inc. 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 JKA.

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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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