FDA 510(k)

BANDAGE, COMPRESSION, FISTULAID

K-Number: K781110 · 1978-08-18

Decision Date1978-08-18

Product CodeDJC

Advisory CommitteeTX

DecisionSubstantially Equivalent

Device Summary

BANDAGE, COMPRESSION, FISTULAID is the device name listed in this FDA 510(k) record. The listed applicant is Medical Device Laboratories. It received FDA 510(k) clearance on 1978-08-18 under 510(k) number K781110. The device is classified under product code DJC. It was reviewed by the TX advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the BANDAGE, COMPRESSION, FISTULAID?

BANDAGE, COMPRESSION, FISTULAID is a medical device that received FDA 510(k) clearance on 1978-08-18. The listed applicant is Medical Device Laboratories. The 510(k) number is K781110.

When did BANDAGE, COMPRESSION, FISTULAID receive FDA 510(k) clearance?

BANDAGE, COMPRESSION, FISTULAID received FDA 510(k) clearance on 1978-08-18, under 510(k) number K781110.

Who is the listed applicant for BANDAGE, COMPRESSION, FISTULAID?

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

What is the FDA product code for BANDAGE, COMPRESSION, FISTULAID?

The FDA product code for BANDAGE, COMPRESSION, FISTULAID is DJC.

Related Clinical Trials

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Other records listing Medical Device Laboratories as applicant

K771573DUO-CATH FEMORAL

Related Devices (Code: DJC)

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.