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FDA 510(k)

DRYSLIDE CEFIN

K-Number: K930702 · 1993-12-22

ApplicantDifco Laboratories, Inc.
Decision Date1993-12-22
Product CodeJTN
Advisory CommitteeMI
DecisionSubstantially Equivalent

Device Summary

DRYSLIDE CEFIN is the device name listed in this FDA 510(k) record. The listed applicant is Difco Laboratories, Inc.. It received FDA 510(k) clearance on 1993-12-22 under 510(k) number K930702. The device is classified under product code JTN. It was reviewed by the MI advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the DRYSLIDE CEFIN?

DRYSLIDE CEFIN is a medical device that received FDA 510(k) clearance on 1993-12-22. The listed applicant is Difco Laboratories, Inc.. The 510(k) number is K930702.

When did DRYSLIDE CEFIN receive FDA 510(k) clearance?

DRYSLIDE CEFIN received FDA 510(k) clearance on 1993-12-22, under 510(k) number K930702.

Who is the listed applicant for DRYSLIDE CEFIN?

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

What is the FDA product code for DRYSLIDE CEFIN?

The FDA product code for DRYSLIDE CEFIN is JTN.

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Other records listing Difco Laboratories, Inc. as applicant

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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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