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FDA 510(k)

BIOGLAS MICROCARRIER BEAD

K-Number: K852506 · 1985-07-12

ApplicantSolohill Engineering, Inc.
Decision Date1985-07-12
Product CodeKJB
Advisory CommitteeHE
DecisionSubstantially Equivalent

Device Summary

BIOGLAS MICROCARRIER BEAD is the device name listed in this FDA 510(k) record. The listed applicant is Solohill Engineering, Inc.. It received FDA 510(k) clearance on 1985-07-12 under 510(k) number K852506. The device is classified under product code KJB. It was reviewed by the HE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BIOGLAS MICROCARRIER BEAD?

BIOGLAS MICROCARRIER BEAD is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is Solohill Engineering, Inc.. The 510(k) number is K852506.

When did BIOGLAS MICROCARRIER BEAD receive FDA 510(k) clearance?

BIOGLAS MICROCARRIER BEAD received FDA 510(k) clearance on 1985-07-12, under 510(k) number K852506.

Who is the listed applicant for BIOGLAS MICROCARRIER BEAD?

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

What is the FDA product code for BIOGLAS MICROCARRIER BEAD?

The FDA product code for BIOGLAS MICROCARRIER BEAD is KJB.

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Related Devices (Code: KJB)

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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