510(K) CLEARANCES 84 ▲14RECALLS POSTED 39 ▲27CLASS I 6 ▲2PMA DECISIONS 47 ▲11WEEK ENDING / FDA DATA AS OF
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K921710Substantially Equivalent

Movit Device

John J. Navar, M.D., Corpus Christi TX / Traditional, Substantially Equivalent
FDA source (opens on fda.gov)

K921710 is the FDA 510(k) clearance record for MOVIT DEVICE, a class I device, cleared for John J. Navar, M.D. on under FDA product code BRY (Cabinet, Table And Tray, Anesthesia). FDA records list one 510(k) clearance for John J. Navar, M.D. As of , FDA records show no recalls naming K921710.

Clearance record

Decision date
Received
(82 days to decision)
Product code
BRY Cabinet, Table And Tray, Anesthesia
Regulation
21 CFR 868.6100
Device class
Class I
Review panel
Anesthesiology
Applicant
John J. Navar, M.D. 337 Claremore, Corpus Christi TX
510(k) summary
Statement
Third party review
No

Clearances, product code BRY

Trailing 12 months

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

FDA records show no clearances under product code BRY in the twelve months to October 2026.
Show the numbers
Monthly 510(k) clearances under FDA product code BRY, 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