510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K770628Substantially Equivalent

Clamp Be-152

Instrumentation Industries, Incorporated, Mchenry IL / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K770628 is the FDA 510(k) clearance record for CLAMP BE-152, a class I device, cleared for Instrumentation Industries, Inc. on under FDA product code JAY (Support, Breathing Tube). FDA records list 45 510(k) clearances for INSTRUMENTATION INDUSTRIES, INCORPORATED, from to . As of , FDA records show no recalls naming K770628.

Clearance record

Decision date
Received
(49 days to decision)
Product code
JAY Support, Breathing Tube
Regulation
21 CFR 868.5280
Device class
Class I
Review panel
Anesthesiology
Applicant
Instrumentation Industries, Inc. 803 N. Front St. Suite 3, Mchenry IL
Third party review
No

Clearances, product code JAY

Trailing 12 months

FDA records hold no clearances under product code JAY in the trailing twelve months.

FDA records show no clearances under product code JAY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code JAY, trailing twelve months
MonthClearances
November 20250
December 20250
January 20260
February 20260
March 20260
April 20260
May 20260
June 20260
July 20260
August 20260
September 20260
October 20260