STREP-SPEC
K-Number: K791991 · 1979-11-13
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Device Summary
Frequently Asked Questions
What is the STREP-SPEC?
STREP-SPEC is a medical device that received FDA 510(k) clearance on 1979-11-13. The listed applicant is Micro-Media Systems, Inc.. The 510(k) number is K791991.
When did STREP-SPEC receive FDA 510(k) clearance?
STREP-SPEC received FDA 510(k) clearance on 1979-11-13, under 510(k) number K791991.
Who is the listed applicant for STREP-SPEC?
The FDA 510(k) record lists Micro-Media Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for STREP-SPEC?
The FDA product code for STREP-SPEC is JSS.
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 Micro-Media Systems, 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: JSS)
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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