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FDA 510(k)

PSEUDO-PALETTE TM

K-Number: K790992 · 1979-06-22

ApplicantMicro-Palettes, Inc.
Decision Date1979-06-22
Product CodeJSW
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

PSEUDO-PALETTE TM is the device name listed in this FDA 510(k) record. The listed applicant is Micro-Palettes, Inc.. It received FDA 510(k) clearance on 1979-06-22 under 510(k) number K790992. The device is classified under product code JSW. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PSEUDO-PALETTE TM?

PSEUDO-PALETTE TM is a medical device that received FDA 510(k) clearance on 1979-06-22. The listed applicant is Micro-Palettes, Inc.. The 510(k) number is K790992.

When did PSEUDO-PALETTE TM receive FDA 510(k) clearance?

PSEUDO-PALETTE TM received FDA 510(k) clearance on 1979-06-22, under 510(k) number K790992.

Who is the listed applicant for PSEUDO-PALETTE TM?

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

What is the FDA product code for PSEUDO-PALETTE TM?

The FDA product code for PSEUDO-PALETTE TM is JSW.

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 Micro-Palettes, 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.

K790991YEAST-PALETTE TM

Related Devices (Code: JSW)

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.

K922768RAPID NFT, MODIFICATIONBiomerieux Vitek, Inc.K900517RAPID NF SYSTEMInnovative Diagnostic Systems, Inc.K870769AUSTIN NONFERMENTER KITAustin Biological LaboratoriesK772112NON-FERMENTER SYSTEMCorning Medical & ScientificK770745PANEL, GNF, MICRO-IDMicro-Media 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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