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Model 366-08 Adaptaid Connector Adapter

by Intermedics, Inc. 510(k)

Active United States

510(k) K860832

Regulatory status

as of 29 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK860832 Date31 Mar 1986ClearedStatusActive

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  • Withdrawn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 11 Oct 2026.

Specification

510(k)

510(k) Number
FDA Product Code
DTD
Device Class
Class II
Regulation
21 CFR Part 870.3620
Advisory Committee
Cardiovascular
FDA Decision
SESE Substantially Equivalent

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