FDA 510(k) Search

Search Filters

Search Everything

510k Number

Type

Panel

Product Code

Subsequent Product Code

Applicant Name (Manufacturer)

Device Name

Device Description

Intended Use

Predicate Devices

Reference Devices

510k Summary Text (Full-text Search)

Decision

Decision Date From

Decision Date To

Third Party Reviewed

Expedited Review

Is SaMD

Contains AI/ML

Is IVD

Is Diagnostic

Is Therapeutic

is PCCP Authorized

Has PDF Data

Sort By

Sort Order

Search Results

Found 2 results

510(k) Data Aggregation

K Number

Device Name

BIRTHDAY KIT (OBSTETRICAL DELIVERY KIT)

Manufacturer

DEVON INDUSTRIES, INC.

Date Cleared

1996-07-03

(43 days)

Product Code

MLS

Regulation Number

884.4530

Why did this record match?

Product Code :

MLS

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

Ask a Question

K Number

Device Name

CPR C-SECTION DELIVERY PACK

Manufacturer

CUSTOM PACK RELIABILITY

Date Cleared

1996-05-23

(128 days)

Product Code

MLS

Regulation Number

884.4530

Why did this record match?

Product Code :

MLS

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticDiagnosticis PCCP Authorized

Intended Use

Device Description

Ask a Question

Page 1 of 1