LOMBARD-DOWELL STARCH AGAR
K-Number: K790618 · 1979-04-23
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Device Summary
Frequently Asked Questions
What is the LOMBARD-DOWELL STARCH AGAR?
LOMBARD-DOWELL STARCH AGAR is a medical device that received FDA 510(k) clearance on 1979-04-23. The listed applicant is Anaerobe Systems. The 510(k) number is K790618.
When did LOMBARD-DOWELL STARCH AGAR receive FDA 510(k) clearance?
LOMBARD-DOWELL STARCH AGAR received FDA 510(k) clearance on 1979-04-23, under 510(k) number K790618.
Who is the listed applicant for LOMBARD-DOWELL STARCH AGAR?
The FDA 510(k) record lists Anaerobe Systems as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for LOMBARD-DOWELL STARCH AGAR?
The FDA product code for LOMBARD-DOWELL STARCH AGAR is JSH.
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 Anaerobe Systems 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: JSH)
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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