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Espree' Guedel Espree Berman Airway

by Esp Plastics, Inc. 510(k)

Active United States

510(k) K821308

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK821308 Date21 May 1982ClearedStatusActive

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  • Withdrawn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
CAE
Device Class
Class I
Regulation
21 CFR Part 868.5110
Advisory Committee
Anesthesiology
FDA Decision
SESE Substantially Equivalent

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