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FDA 510(k)

CARBON FIBER CONFORMAL COUCH TOP

K-Number: K973842 · 1997-12-05

ApplicantMedtec, Inc.
Decision Date1997-12-05
Product CodeIXQ
Advisory CommitteeRA
DecisionSubstantially Equivalent

Device Summary

CARBON FIBER CONFORMAL COUCH TOP is the device name listed in this FDA 510(k) record. The listed applicant is Medtec, Inc.. It received FDA 510(k) clearance on 1997-12-05 under 510(k) number K973842. The device is classified under product code IXQ. It was reviewed by the RA advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CARBON FIBER CONFORMAL COUCH TOP?

CARBON FIBER CONFORMAL COUCH TOP is a medical device that received FDA 510(k) clearance on 1997-12-05. The listed applicant is Medtec, Inc.. The 510(k) number is K973842.

When did CARBON FIBER CONFORMAL COUCH TOP receive FDA 510(k) clearance?

CARBON FIBER CONFORMAL COUCH TOP received FDA 510(k) clearance on 1997-12-05, under 510(k) number K973842.

Who is the listed applicant for CARBON FIBER CONFORMAL COUCH TOP?

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

What is the FDA product code for CARBON FIBER CONFORMAL COUCH TOP?

The FDA product code for CARBON FIBER CONFORMAL COUCH TOP is IXQ.

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.

Other records listing Medtec, 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.

View all 40 devices →

Related Devices (Code: IXQ)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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