GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.
K-Number: K873257 · 1987-11-06
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Device Summary
Frequently Asked Questions
What is the GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.?
GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is Central Media. The 510(k) number is K873257.
When did GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. receive FDA 510(k) clearance?
GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873257.
Who is the listed applicant for GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.?
The FDA 510(k) record lists Central Media as the applicant. This does not by itself establish the device manufacturer.
What is the FDA product code for GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.?
The FDA product code for GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. is JSG.
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 Central Media 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: JSG)
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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