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FDA 510(k)

CAP 400 AT

K-Number: K935272 · 1994-07-13

ApplicantPryon Corp.
Decision Date1994-07-13
Product CodeCCK
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

CAP 400 AT is the device name listed in this FDA 510(k) record. The listed applicant is Pryon Corp.. It received FDA 510(k) clearance on 1994-07-13 under 510(k) number K935272. The device is classified under product code CCK. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the CAP 400 AT?

CAP 400 AT is a medical device that received FDA 510(k) clearance on 1994-07-13. The listed applicant is Pryon Corp.. The 510(k) number is K935272.

When did CAP 400 AT receive FDA 510(k) clearance?

CAP 400 AT received FDA 510(k) clearance on 1994-07-13, under 510(k) number K935272.

Who is the listed applicant for CAP 400 AT?

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

What is the FDA product code for CAP 400 AT?

The FDA product code for CAP 400 AT is CCK.

Other records listing Pryon Corp. 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.

Related Devices (Code: CCK)

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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