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FDA 510(k)

ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES

K-Number: K882741 · 1988-08-30

Decision Date1988-08-30
Product CodeCKG
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES is the device name listed in this FDA 510(k) record. The listed applicant is Nichols Institute Diagnostics. It received FDA 510(k) clearance on 1988-08-30 under 510(k) number K882741. The device is classified under product code CKG. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES?

ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES is a medical device that received FDA 510(k) clearance on 1988-08-30. The listed applicant is Nichols Institute Diagnostics. The 510(k) number is K882741.

When did ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES receive FDA 510(k) clearance?

ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES received FDA 510(k) clearance on 1988-08-30, under 510(k) number K882741.

Who is the listed applicant for ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES?

The FDA 510(k) record lists Nichols Institute Diagnostics as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES?

The FDA product code for ALLEGRO ACTH IMMUNOASSAY KIT 65 AND 130 TUBES is CKG.

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 Nichols Institute Diagnostics 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 68 devices →

Related Devices (Code: CKG)

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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