Atlas FDA

PERI-BOTTLE

FDA 510(k) clearance K902830 · decided 1990-08-06

Clearance details

K-number
K902830
Device name
PERI-BOTTLE
Applicant
Orion Life Systems, Inc.
Decision
Substantially Equivalent
Date received
1990-06-28
Decision date
1990-08-06
Days to decision
39 days
Clearance type
Traditional
Product code
HED
Device class
1
Regulation number
884.5900
Medical specialty
Obstetrics/Gynecology
Advisory committee
Obstetrics/Gynecology
Location
Wheeling, IL, 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
WATER WORKS DOUCHING DEVICE (K080200)Abbott Research Group, Inc.2008-07-10
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LA JOIE (K000736)Goomi Ehwa, Inc.2000-08-08
GENT-L-KARE VAGINAL IRRIGATION SET (K881216)Geneva Laboratories, Inc.1988-06-07
P.A. MEDICAL VAGINAL IRRIGATION SET #1130 (K854595)Pa Medical Corp.1986-01-13
MAC LEE VAGINAL IRRIGATOR (K841710)Mac Lee Medical Products1984-06-19
FEMININE HYGIENE DEVICE (K831667)Snow Willow Co.1983-09-12
DOUCHE TRAY-DISPOS. VAGINAL TRAY W/POVID (K800954)The Healthcare Group Laboratories, Inc.1980-10-03
DOUCH TRAY-DISPOSABLE VAGINAL TRAY W/BEN (K800956)The Healthcare Group Laboratories, Inc.1980-10-03
DOUCHE UNIT-1500 ML DISP. CONTAINER (K800957)The Healthcare Group Laboratories, Inc.1980-07-14
DOUCHE KIT, SOMETHING PERSONAL (K781207)Chatten Drug & Chemical Co.1978-08-10

Recalls involving this device

No recalls on record reference this clearance.