STAK-CHEX PLUS RETICS
K-Number: K992887 · 1999-11-22
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Device Summary
Frequently Asked Questions
What is the STAK-CHEX PLUS RETICS?
STAK-CHEX PLUS RETICS is a medical device that received FDA 510(k) clearance on 1999-11-22. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K992887.
When did STAK-CHEX PLUS RETICS receive FDA 510(k) clearance?
STAK-CHEX PLUS RETICS received FDA 510(k) clearance on 1999-11-22, under 510(k) number K992887.
Who is the listed applicant for STAK-CHEX PLUS RETICS?
The FDA 510(k) record lists Streck Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STAK-CHEX PLUS RETICS?
The FDA product code for STAK-CHEX PLUS RETICS is GLQ.
Related Clinical Trials
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.
Other records listing Streck Laboratories, Inc. 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.
Related Devices (Code: GLQ)
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.
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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