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Found 4 results

510(k) Data Aggregation

K Number

Validate with FDA (Live)

Device Name

THE TULIP LAPAROSCOPE SHEATH 6MM DUAL STOPCOCK

Manufacturer

THE TULIP MFG. CO.

Date Cleared

1996-01-22

(210 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

THE TULIP LAPAROSCOPE SHEATH 6MM SINGLE STOPCOCK

Manufacturer

THE TULIP MFG. CO.

Date Cleared

1996-01-22

(213 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

THE TULIP MONO POLAR ROTATABLE METZ SCISSORS

Manufacturer

THE TULIP MFG. CO.

Date Cleared

1996-01-17

(47 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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K Number

Validate with FDA (Live)

Device Name

THE TULIP MONO POLAR ROTATABLE ALLIGATOR FORCEP

Manufacturer

THE TULIP MFG. CO.

Date Cleared

1996-01-17

(47 days)

Product Code

Regulation Number

Type

Panel

General & Plastic Surgery

Age Range

N/A

Reference & Predicate Devices

N/A

Predicate For

N/A

AI/MLSaMDIVD (In Vitro Diagnostic)TherapeuticPediatricDiagnosticis PCCP AuthorizedThirdpartyExpeditedreview

Intended Use

Device Description

AI/ML Overview

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