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FDA 510(k)

SEPACELL R-500 AND SEPACELL R-500A

K-Number: K873792 · 1988-01-19

Decision Date1988-01-19
Product CodeCAK
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

SEPACELL R-500 AND SEPACELL R-500A is the device name listed in this FDA 510(k) record. The listed applicant is Advocacy International, Ltd.. It received FDA 510(k) clearance on 1988-01-19 under 510(k) number K873792. The device is classified under product code CAK. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SEPACELL R-500 AND SEPACELL R-500A?

SEPACELL R-500 AND SEPACELL R-500A is a medical device that received FDA 510(k) clearance on 1988-01-19. The listed applicant is Advocacy International, Ltd.. The 510(k) number is K873792.

When did SEPACELL R-500 AND SEPACELL R-500A receive FDA 510(k) clearance?

SEPACELL R-500 AND SEPACELL R-500A received FDA 510(k) clearance on 1988-01-19, under 510(k) number K873792.

Who is the listed applicant for SEPACELL R-500 AND SEPACELL R-500A?

The FDA 510(k) record lists Advocacy International, Ltd. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SEPACELL R-500 AND SEPACELL R-500A?

The FDA product code for SEPACELL R-500 AND SEPACELL R-500A is CAK.

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 Advocacy International, Ltd. 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 13 devices →

Related Devices (Code: CAK)

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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