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FDA 510(k)

APL MARTIN LEWIS MEDIUM

K-Number: K853237 · 1985-08-19

ApplicantApl Medical Supplies
Decision Date1985-08-19
Product CodeJTY
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

APL MARTIN LEWIS MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Apl Medical Supplies. It received FDA 510(k) clearance on 1985-08-19 under 510(k) number K853237. 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 APL MARTIN LEWIS MEDIUM?

APL MARTIN LEWIS MEDIUM is a medical device that received FDA 510(k) clearance on 1985-08-19. The listed applicant is Apl Medical Supplies. The 510(k) number is K853237.

When did APL MARTIN LEWIS MEDIUM receive FDA 510(k) clearance?

APL MARTIN LEWIS MEDIUM received FDA 510(k) clearance on 1985-08-19, under 510(k) number K853237.

Who is the listed applicant for APL MARTIN LEWIS MEDIUM?

The FDA 510(k) record lists Apl Medical Supplies as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for APL MARTIN LEWIS MEDIUM?

The FDA product code for APL MARTIN LEWIS MEDIUM is JTY.

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Other records listing Apl Medical Supplies 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.

K853618APL SIM MEDIUMK853610APL MOTILITY INDOLE ORNITHINE AGARK853617APL SIMMONS CITRATE AGARK853619APL TRIPLE SUGAR IRON AGARK853609APL TRYPTIC SOY BROTHK853611APL XYLOSE LYSINE DEOXYCHOLATE AGAR

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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.

K210511InTray GCBiomed Diagnostics IncorporatedK993033INTRAY GCBiomed Diagnostics, Inc.K954986GC BASE W/ 1% GCHIRemel, L.P.K950196CULTURE MEDIA, FOR ISOLATION OF PATHOGENIC NEISSERIABioclinical Systems, Inc.K933122MICROBIOLOGICAL CULTURE MEDIA,MARTIN LEWIS AGARBioclinical Systems, Inc.K933121MICROBIOLOGICAL CULTURE MEDIA,CHOCOLATE AGARBioclinical Systems, Inc.

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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