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FDA 510(k)

MC ACCLAIM Q6000 BED

K-Number: K951161 · 1995-05-09

ApplicantJanco Consulting Services
Decision Date1995-05-09
Product CodeFNL
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

MC ACCLAIM Q6000 BED is the device name listed in this FDA 510(k) record. The listed applicant is Janco Consulting Services. It received FDA 510(k) clearance on 1995-05-09 under 510(k) number K951161. The device is classified under product code FNL. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the MC ACCLAIM Q6000 BED?

MC ACCLAIM Q6000 BED is a medical device that received FDA 510(k) clearance on 1995-05-09. The listed applicant is Janco Consulting Services. The 510(k) number is K951161.

When did MC ACCLAIM Q6000 BED receive FDA 510(k) clearance?

MC ACCLAIM Q6000 BED received FDA 510(k) clearance on 1995-05-09, under 510(k) number K951161.

Who is the listed applicant for MC ACCLAIM Q6000 BED?

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

What is the FDA product code for MC ACCLAIM Q6000 BED?

The FDA product code for MC ACCLAIM Q6000 BED is FNL.

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.

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Other records listing Janco Consulting Services 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.

K950059MC INFANT CARE UNIE #PP30K950058MC HEALTHCARE #CH31 CHILD'S CRIB

Related Devices (Code: FNL)

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.

K202964iBed Wireless with iBed MobileStryker CorporationK103536IBED WIRELESS WITH IBED AWARENESSStryker CorporationK982783VAIL 1000 ENCLOSED BEDVail Products, Inc.K974296MODEL 720 SERIES FULL/SEMI ELECTRIC BED 1120 FULL ELECTRIC BEDInvacare Corp.K974254BENEFIT B3--- SERIESM.C. Healthcare Products, Inc.K972115VOLKER HOSPITAL BED, MODEL K960Volker Healthcare, 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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