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FDA 510(k)

AMS GRAM-NEGATIVE IDENT. CARD

K-Number: K834269 · 1984-03-09

ApplicantVitek Systems, Inc.
Decision Date1984-03-09
Product CodeJTO
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

AMS GRAM-NEGATIVE IDENT. CARD is the device name listed in this FDA 510(k) record. The listed applicant is Vitek Systems, Inc.. It received FDA 510(k) clearance on 1984-03-09 under 510(k) number K834269. The device is classified under product code JTO. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMS GRAM-NEGATIVE IDENT. CARD?

AMS GRAM-NEGATIVE IDENT. CARD is a medical device that received FDA 510(k) clearance on 1984-03-09. The listed applicant is Vitek Systems, Inc.. The 510(k) number is K834269.

When did AMS GRAM-NEGATIVE IDENT. CARD receive FDA 510(k) clearance?

AMS GRAM-NEGATIVE IDENT. CARD received FDA 510(k) clearance on 1984-03-09, under 510(k) number K834269.

Who is the listed applicant for AMS GRAM-NEGATIVE IDENT. CARD?

The FDA 510(k) record lists Vitek Systems, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AMS GRAM-NEGATIVE IDENT. CARD?

The FDA product code for AMS GRAM-NEGATIVE IDENT. CARD is JTO.

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Related Devices (Code: JTO)

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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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