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FDA 510(k)

SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM

K-Number: K871855 · 1987-05-26

ApplicantGibco Laboratories Life Technologies, Inc.
Decision Date1987-05-26
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM is the device name listed in this FDA 510(k) record. The listed applicant is Gibco Laboratories Life Technologies, Inc.. It received FDA 510(k) clearance on 1987-05-26 under 510(k) number K871855. 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 SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM?

SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM is a medical device that received FDA 510(k) clearance on 1987-05-26. The listed applicant is Gibco Laboratories Life Technologies, Inc.. The 510(k) number is K871855.

When did SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM receive FDA 510(k) clearance?

SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM received FDA 510(k) clearance on 1987-05-26, under 510(k) number K871855.

Who is the listed applicant for SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM?

The FDA 510(k) record lists Gibco Laboratories Life Technologies, Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM?

The FDA product code for SORBITOL MACCONKEY (SMAC) AGAR, DRI & PRE-FORM is JSH.

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Other records listing Gibco Laboratories Life Technologies, Inc. as applicant

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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.

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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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