CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS
K-Number: K851372 · 1985-07-12
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Device Summary
Frequently Asked Questions
What is the CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS?
CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS is a medical device that received FDA 510(k) clearance on 1985-07-12. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K851372.
When did CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS receive FDA 510(k) clearance?
CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS received FDA 510(k) clearance on 1985-07-12, under 510(k) number K851372.
Who is the listed applicant for CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS?
The FDA 510(k) record lists Difco Laboratories, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS?
The FDA product code for CELLMATICS HERPES SIMPLEX VIRUS DETECT-SYS is GQL.
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 Difco 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: GQL)
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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