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FDA 510(k)

COUNT-A-DOSE

K-Number: K883311 · 1988-09-15

ApplicantPavel Jordan & Associates, Inc.
Decision Date1988-09-15
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

COUNT-A-DOSE is the device name listed in this FDA 510(k) record. The listed applicant is Pavel Jordan & Associates, Inc.. It received FDA 510(k) clearance on 1988-09-15 under 510(k) number K883311. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the COUNT-A-DOSE?

COUNT-A-DOSE is a medical device that received FDA 510(k) clearance on 1988-09-15. The listed applicant is Pavel Jordan & Associates, Inc.. The 510(k) number is K883311.

When did COUNT-A-DOSE receive FDA 510(k) clearance?

COUNT-A-DOSE received FDA 510(k) clearance on 1988-09-15, under 510(k) number K883311.

Who is the listed applicant for COUNT-A-DOSE?

The FDA 510(k) record lists Pavel Jordan & Associates, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for COUNT-A-DOSE?

The FDA product code for COUNT-A-DOSE is FMF.

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.

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Other records listing Pavel Jordan & Associates, Inc. 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.

K883164INSTAJECT IIK870474INSTAJECT

Related Devices (Code: FMF)

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.

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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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