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FDA 510(k)

CONVERTA-LITTER

K-Number: K874060 · 1987-12-10

ApplicantCamtec
Decision Date1987-12-10
Product CodeINN
Advisory CommitteePM
DecisionSubstantially Equivalent

Device Summary

CONVERTA-LITTER is the device name listed in this FDA 510(k) record. The listed applicant is Camtec. It received FDA 510(k) clearance on 1987-12-10 under 510(k) number K874060. The device is classified under product code INN. It was reviewed by the PM advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CONVERTA-LITTER?

CONVERTA-LITTER is a medical device that received FDA 510(k) clearance on 1987-12-10. The listed applicant is Camtec. The 510(k) number is K874060.

When did CONVERTA-LITTER receive FDA 510(k) clearance?

CONVERTA-LITTER received FDA 510(k) clearance on 1987-12-10, under 510(k) number K874060.

Who is the listed applicant for CONVERTA-LITTER?

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

What is the FDA product code for CONVERTA-LITTER?

The FDA product code for CONVERTA-LITTER is INN.

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 Camtec 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.

K872729INFUSION STAND

Related Devices (Code: INN)

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.

K945650SPIFFYThames Valley Children'S CentreK942397THERADAPT HIGHCHAIR/STROLLER INSERTTheradapt Products, Inc.K930520THERADAPT(R) ADJUSTABLE CLASSROOM CHAIRTheradapt Products, Inc.K923750ABLE GENERATION BOOSTER CHAIRThe Able Generation, Inc.K923752ABLE GENERATION PLAY CHAIRThe Able Generation, Inc.K923753ABLE GENERATION THERAPY TILT BENCHThe Able Generation, 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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