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Spand-Gel Granulated Gel

by Medi-Tech Intl. Corp. 510(k)

Active United States

510(k) K864124

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SN Traditional NumberK864124 Date26 Nov 1986DecidedStatusActive

Coverage

1 jurisdiction

United States of America
  • Active
  • Expiring
  • Withdrawn
  • Listed
  • Not covered

United States — FDA 510(k) Active

Recalls

0 recalls · FDA

No FDA recalls on record, checked 22 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
KMF
Device Class
Class I
Regulation
21 CFR Part 880.5090
Advisory Committee
General Hospital
FDA Decision
SN

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