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FDA 510(k)

SPECIMEN TRANSPORT MEDIUM

K-Number: K935618 · 1994-04-21

Decision Date1994-04-21
Product CodeJSM
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

SPECIMEN TRANSPORT MEDIUM is the device name listed in this FDA 510(k) record. The listed applicant is Biowhittaker Molecular Applications, Inc.. It received FDA 510(k) clearance on 1994-04-21 under 510(k) number K935618. The device is classified under product code JSM. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SPECIMEN TRANSPORT MEDIUM?

SPECIMEN TRANSPORT MEDIUM is a medical device that received FDA 510(k) clearance on 1994-04-21. The listed applicant is Biowhittaker Molecular Applications, Inc.. The 510(k) number is K935618.

When did SPECIMEN TRANSPORT MEDIUM receive FDA 510(k) clearance?

SPECIMEN TRANSPORT MEDIUM received FDA 510(k) clearance on 1994-04-21, under 510(k) number K935618.

Who is the listed applicant for SPECIMEN TRANSPORT MEDIUM?

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

What is the FDA product code for SPECIMEN TRANSPORT MEDIUM?

The FDA product code for SPECIMEN TRANSPORT MEDIUM is JSM.

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 Biowhittaker Molecular Applications, 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 10 devices →

Related Devices (Code: JSM)

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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