RETIC-CHEX
K-Number: K843093 · 1984-10-23
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Device Summary
Frequently Asked Questions
What is the RETIC-CHEX?
RETIC-CHEX is a medical device that received FDA 510(k) clearance on 1984-10-23. The listed applicant is Streck Laboratories, Inc.. The 510(k) number is K843093.
When did RETIC-CHEX receive FDA 510(k) clearance?
RETIC-CHEX received FDA 510(k) clearance on 1984-10-23, under 510(k) number K843093.
Who is the listed applicant for RETIC-CHEX?
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 RETIC-CHEX?
The FDA product code for RETIC-CHEX is JPK.
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: JPK)
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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