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FDA 510(k)

ACETAMIDE AGAR SLANTS

K-Number: K834509 · 1984-01-27

Decision Date1984-01-27
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

ACETAMIDE AGAR SLANTS is the device name listed in this FDA 510(k) record. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. It received FDA 510(k) clearance on 1984-01-27 under 510(k) number K834509. The device is classified under product code JSH. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ACETAMIDE AGAR SLANTS?

ACETAMIDE AGAR SLANTS is a medical device that received FDA 510(k) clearance on 1984-01-27. The listed applicant is Bd Becton Dickinson Vacutainer Systems Preanalytic. The 510(k) number is K834509.

When did ACETAMIDE AGAR SLANTS receive FDA 510(k) clearance?

ACETAMIDE AGAR SLANTS received FDA 510(k) clearance on 1984-01-27, under 510(k) number K834509.

Who is the listed applicant for ACETAMIDE AGAR SLANTS?

The FDA 510(k) record lists Bd Becton Dickinson Vacutainer Systems Preanalytic as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ACETAMIDE AGAR SLANTS?

The FDA product code for ACETAMIDE AGAR SLANTS is JSH.

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 Bd Becton Dickinson Vacutainer Systems Preanalytic 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 632 devices →

Related Devices (Code: JSH)

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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