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FDA 510(k)

MARTIN LEWIS AGAR (JEMBEC)

K-Number: K771870 · 1977-10-25

Decision Date1977-10-25
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

MARTIN LEWIS AGAR (JEMBEC) is the device name listed in this FDA 510(k) record. The listed applicant is Granite Diagnostics, Inc.. It received FDA 510(k) clearance on 1977-10-25 under 510(k) number K771870. The device is classified under product code JTY. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MARTIN LEWIS AGAR (JEMBEC)?

MARTIN LEWIS AGAR (JEMBEC) is a medical device that received FDA 510(k) clearance on 1977-10-25. The listed applicant is Granite Diagnostics, Inc.. The 510(k) number is K771870.

When did MARTIN LEWIS AGAR (JEMBEC) receive FDA 510(k) clearance?

MARTIN LEWIS AGAR (JEMBEC) received FDA 510(k) clearance on 1977-10-25, under 510(k) number K771870.

Who is the listed applicant for MARTIN LEWIS AGAR (JEMBEC)?

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

What is the FDA product code for MARTIN LEWIS AGAR (JEMBEC)?

The FDA product code for MARTIN LEWIS AGAR (JEMBEC) is JTY.

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 Granite Diagnostics, 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.

View all 47 devices →

Related Devices (Code: JTY)

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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