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FDA 510(k)

KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR

K-Number: K853797 · 1985-10-07

ApplicantCedar Surgical, Inc.
Decision Date1985-10-07
Product Code
DecisionSubstantially Equivalent

Device Summary

KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR is the device name listed in this FDA 510(k) record. The listed applicant is Cedar Surgical, Inc.. It received FDA 510(k) clearance on 1985-10-07 under 510(k) number K853797. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR?

KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR is a medical device that received FDA 510(k) clearance on 1985-10-07. The listed applicant is Cedar Surgical, Inc.. The 510(k) number is K853797.

When did KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR receive FDA 510(k) clearance?

KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR received FDA 510(k) clearance on 1985-10-07, under 510(k) number K853797.

Who is the listed applicant for KNEELING ATTACHMENT & CUSHIONED FACE REST SYS FOR?

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

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Other records listing Cedar Surgical, 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.

K873692RAYLOR(TM) DRILL STOPK872281RAYLOR FUSION FUNNELK873690CEDAR(TM) PELVIC CUSHIONK873691CEDAR(TM) RETRACTOR RINGK864425RAYLOR(TM) DISSECTING HOOKK864421RAYLOR(TM) PERIOSTEAL ELEVATORS

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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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