HOBBS MEDICAL MICROBIOLOGY BRUSH
K-Number: K893729 · 1989-08-28
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Device Summary
Frequently Asked Questions
What is the HOBBS MEDICAL MICROBIOLOGY BRUSH?
HOBBS MEDICAL MICROBIOLOGY BRUSH is a medical device that received FDA 510(k) clearance on 1989-08-28. The listed applicant is Hobbs Medical, Inc.. The 510(k) number is K893729.
When did HOBBS MEDICAL MICROBIOLOGY BRUSH receive FDA 510(k) clearance?
HOBBS MEDICAL MICROBIOLOGY BRUSH received FDA 510(k) clearance on 1989-08-28, under 510(k) number K893729.
Who is the listed applicant for HOBBS MEDICAL MICROBIOLOGY BRUSH?
The FDA 510(k) record lists Hobbs Medical, Inc. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for HOBBS MEDICAL MICROBIOLOGY BRUSH?
The FDA product code for HOBBS MEDICAL MICROBIOLOGY BRUSH is FDX.
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 Hobbs Medical, 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: FDX)
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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