DIPSTICK SALMONELLA
K-Number: K910438 · 1991-09-13
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Device Summary
Frequently Asked Questions
What is the DIPSTICK SALMONELLA?
DIPSTICK SALMONELLA is a medical device that received FDA 510(k) clearance on 1991-09-13. The listed applicant is Ampcor, Inc.. The 510(k) number is K910438.
When did DIPSTICK SALMONELLA receive FDA 510(k) clearance?
DIPSTICK SALMONELLA received FDA 510(k) clearance on 1991-09-13, under 510(k) number K910438.
Who is the listed applicant for DIPSTICK SALMONELLA?
The FDA 510(k) record lists Ampcor, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for DIPSTICK SALMONELLA?
The FDA product code for DIPSTICK SALMONELLA is GRM.
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 Ampcor, 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: GRM)
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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