# K974032: Rocket Mucus Sampler Syringe, Sterile, Rocket Mucus Sampler Syringe, Clinically Aspirator

- Pathway: 510(k) (Traditional)
- Applicant: A & A Medical, Inc.
- Decided: Dec 22, 1997 after 60 days
- Product code: HFC (Aspirator, Endocervical)
- Device class: 2
- Regulation: 21 CFR 884.1050
- Recalls of this device: none
- Data: FDA decisions to Oct 25, 2026; recalls to Oct 12, 2026

## Lineage
No predicates in its family tree.
No later device cites it as a predicate yet.
0 of 1 device in its family (counting itself) have a Class I recall.

## Predicates on the family tree (from the FDA summary)
- None. The FDA summary names its predicate without a number.
- (no number) Aspirette Endocervical Aspirator from Unimar, Inc.: named in the summary without a submission number
- (no number) SelectMucus from Select Medical Systems, Inc: named in the summary without a submission number
- (no number) Cervical Mucous Aspiration Catheter from Cook Urological, Inc: named in the summary without a submission number

## Indications for use
The Rocket Mucus Sampler is designed for optimum suction for the collection of cervical mucosal lining, post coital test (Huhner), external os or vaginal pool sampling. The Rocket Mucous Sampler enables the Ob/Gyn physician to collect the specimen and send it to the laboratory to be examined histologically or cytologically

Source page: https://510kreport.com/device/K974032
Methodology: https://510kreport.com/methodology