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FDA 510(k)

ADAPTIC* C.F.S.

K-Number: K812449 · 1981-09-25

ApplicantJohnson & Johnson Professionals, Inc.
Decision Date1981-09-25
Product CodeEBF
Advisory CommitteeDE
DecisionSubstantially Equivalent

Device Summary

ADAPTIC* C.F.S. is the device name listed in this FDA 510(k) record. The listed applicant is Johnson & Johnson Professionals, Inc.. It received FDA 510(k) clearance on 1981-09-25 under 510(k) number K812449. The device is classified under product code EBF. It was reviewed by the DE advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ADAPTIC* C.F.S.?

ADAPTIC* C.F.S. is a medical device that received FDA 510(k) clearance on 1981-09-25. The listed applicant is Johnson & Johnson Professionals, Inc.. The 510(k) number is K812449.

When did ADAPTIC* C.F.S. receive FDA 510(k) clearance?

ADAPTIC* C.F.S. received FDA 510(k) clearance on 1981-09-25, under 510(k) number K812449.

Who is the listed applicant for ADAPTIC* C.F.S.?

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

What is the FDA product code for ADAPTIC* C.F.S.?

The FDA product code for ADAPTIC* C.F.S. is EBF.

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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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