CULTURE COLLECTION DEVICE
K-Number: K881105 · 1988-04-25
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Device Summary
Frequently Asked Questions
What is the CULTURE COLLECTION DEVICE?
CULTURE COLLECTION DEVICE is a medical device that received FDA 510(k) clearance on 1988-04-25. The listed applicant is Medical Packaging Corp.. The 510(k) number is K881105.
When did CULTURE COLLECTION DEVICE receive FDA 510(k) clearance?
CULTURE COLLECTION DEVICE received FDA 510(k) clearance on 1988-04-25, under 510(k) number K881105.
Who is the listed applicant for CULTURE COLLECTION DEVICE?
The FDA 510(k) record lists Medical Packaging Corp. as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for CULTURE COLLECTION DEVICE?
The FDA product code for CULTURE COLLECTION DEVICE is JSM.
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 Medical Packaging Corp. 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: JSM)
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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