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FDA 510(k)

AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE

K-Number: K873359 · 1987-11-06

ApplicantAmerican Pharmaseal Div. Ahsc
Decision Date1987-11-06
Product CodeCAI
Advisory CommitteeAN
DecisionSubstantially Equivalent

Device Summary

AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE is the device name listed in this FDA 510(k) record. The listed applicant is American Pharmaseal Div. Ahsc. It received FDA 510(k) clearance on 1987-11-06 under 510(k) number K873359. The device is classified under product code CAI. It was reviewed by the AN advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE?

AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE is a medical device that received FDA 510(k) clearance on 1987-11-06. The listed applicant is American Pharmaseal Div. Ahsc. The 510(k) number is K873359.

When did AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE receive FDA 510(k) clearance?

AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE received FDA 510(k) clearance on 1987-11-06, under 510(k) number K873359.

Who is the listed applicant for AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE?

The FDA 510(k) record lists American Pharmaseal Div. Ahsc as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE?

The FDA product code for AIRLIFE VOLUME VENTI. CIRCUIT W/CLEAR CAP EX VALVE is CAI.

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Other records listing American Pharmaseal Div. Ahsc as applicant

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K874022PHARMASEAL WOUND IRRIGATION DEVICEK874517PHARMASEAL RUBBER URETHRAL CATHETERK874045PHARMASEAL ENDOSCOPY PREP KIT UPPER AND LOWERK872228PHARMASEAL ALTERNATING PRESSURE PAD SYSTEMK872917JINOTTI SUCTION/OXYGEN INSUFFLATION CATHETERK871429ANTIMICROBIAL FOLEY CATHETER

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Related Devices (Code: CAI)

Related records are matched automatically using names, product codes, or other metadata. A match does not establish a verified clinical, scientific, corporate, or regulatory relationship; review the linked official sources.

K954480CONDENSATE COLLECTION KITNova-VentrxK953787UNICOR, INC. ADULT ANESTHESIA BREATHING CIRCUITUnicor, Inc.K953788UNICOR, INC. GAS SAMPLING LINES & CONNECTORSUnicor, Inc.K952016PRIMA PEDIATRIC GAS SAMPLING CIRCUITSPrima, Inc.K952018PRIMA COAXIAL CIRCUITSPrima, Inc.K952020PRIMA PEDIATRIC ANESTHESIA CIRCUITSPrima, Inc.

Official Source

View on FDA Database →

Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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