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FDA 510(k)

THERMOSTABLE NUCLEASE TEST AGAR

K-Number: K864454 · 1986-11-28

ApplicantDimed, Intl.
Decision Date1986-11-28
Product CodeJSH
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

THERMOSTABLE NUCLEASE TEST AGAR is the device name listed in this FDA 510(k) record. The listed applicant is Dimed, Intl.. It received FDA 510(k) clearance on 1986-11-28 under 510(k) number K864454. 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 THERMOSTABLE NUCLEASE TEST AGAR?

THERMOSTABLE NUCLEASE TEST AGAR is a medical device that received FDA 510(k) clearance on 1986-11-28. The listed applicant is Dimed, Intl.. The 510(k) number is K864454.

When did THERMOSTABLE NUCLEASE TEST AGAR receive FDA 510(k) clearance?

THERMOSTABLE NUCLEASE TEST AGAR received FDA 510(k) clearance on 1986-11-28, under 510(k) number K864454.

Who is the listed applicant for THERMOSTABLE NUCLEASE TEST AGAR?

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

What is the FDA product code for THERMOSTABLE NUCLEASE TEST AGAR?

The FDA product code for THERMOSTABLE NUCLEASE TEST AGAR is JSH.

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.

NCT07608549FLASH Pilot Phase 1 Safety StudyNOT_YET_RECRUITINGNCT06562205PAP Systems External Clinical Studies (ECS)NOT_YET_RECRUITINGNCT06443177The Effect of Sympathetic Modulation on Cerebral Vasospasm Secondary to Aneurysmal Subarachnoid HemorrhageSUSPENDEDNCT07095751Artificial Intelligence-assisted Uro-Cam Catheter Assessment System for Diagnosing Bladder CancerNOT_YET_RECRUITING

Other records listing Dimed, Intl. 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.

K870373STERILE PROCEDURAL TRAYSK862577LINEN (HUCK) TOWEL

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.

K881553RUSSELL DOUBLE SUGAR AGARAcumedia Manufacturers, Inc.K881559UREA AGAR BASEAcumedia Manufacturers, Inc.K881486DNASE TEST AGARAcumedia Manufacturers, Inc.K881540FLO AGARAcumedia Manufacturers, Inc.K881551PHENOL RED BROTH BASEAcumedia Manufacturers, Inc.K881560UREA BROTHAcumedia Manufacturers, 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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