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FDA 510(k)

GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA.

K-Number: K873257 · 1987-11-06

ApplicantCentral Media
Decision Date1987-11-06
Product CodeJSG
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

GENERAL PURPOSE MEDIA W/SELECT. & DIFF. MODIFICA. is the device name listed in this FDA 510(k) record. The listed applicant is Central Media. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873257. The device is classified under product code JSG. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

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.

View all 14 devices →

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

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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