Atlas FDA

INVOTEC MICROSCOPE DRAPE

FDA 510(k) clearance K911040 · decided 1991-06-03

Clearance details

K-number
K911040
Device name
INVOTEC MICROSCOPE DRAPE
Applicant
Invotec International, Inc.
Decision
Substantially Equivalent
Date received
1991-03-08
Decision date
1991-06-03
Days to decision
87 days
Clearance type
Traditional
Product code
HMW
Device class
2
Regulation number
878.4370
Medical specialty
General, Plastic Surgery
Advisory committee
General, Plastic Surgery
Location
Jacksonville, FL, US
Third-party review
No
Expedited review
No

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Similar devices under this product code

Devices cleared under the same product code - the starting set for predicate research.

RecordFirmDate
STERILE INSTRUMENT DRAPE (K902763)North American Sterilization & Packaging Co.1990-09-20
MICROSCOPE DRAPE (K902851)Medical Technique Instruments, Inc.1990-09-10
CUSTOM INSTRUMENT DRAPE (K843890)Lifestream Int'L, Inc.1984-10-26

Recalls involving this device

No recalls on record reference this clearance.