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Record, Model 702, I.L.

by Instrumentation Laboratory CO

510(k) K770946

Record, Model 702, I.L. is a medical device (FDA Class I; FDA product code DSF, Recorder, Paper Chart) made by Instrumentation Laboratory CO, cleared under FDA 510(k) K770946 on 5 Jul 1977, active as of 22 Oct 2026.

Active United States

510(k)

Valid until

No expiry

510(k) clearance is not time-limited

FDA recalls

None found

in data synced 22 Oct 2026

Documents

Trust

Unverified

Source FDA 510(k), synced 22 Oct 2026.

Regulatory status

as of registry sync 22 Oct 2026

RegionAuthorizationNumberDateStatus
United StatesFDA 510(k)SESE Substantially Equivalent · Traditional NumberK770946 Date5 Jul 1977ClearedStatusActive

Official records

Coverage

1 jurisdiction

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  • Withdrawn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

United States — FDA 510(k) Active

Specification

510(k)

510(k) Number
FDA product code
DSF
Device class
Class I
Regulation
21 CFR Part 870.2810
Advisory committee
Cardiovascular
FDA decision
SESE Substantially Equivalent

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Other devices filed under FDA product code DSF (Recorder, Paper Chart).

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