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FDA 510(k)

PAB CONVENIENCE TRAY

K-Number: K781264 · 1978-09-20

ApplicantWaters Assoc., Inc.
Decision Date1978-09-20
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

PAB CONVENIENCE TRAY is the device name listed in this FDA 510(k) record. The listed applicant is Waters Assoc., Inc.. It received FDA 510(k) clearance on 1978-09-20 under 510(k) number K781264. The device is classified under product code GAA. It was reviewed by the SU advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PAB CONVENIENCE TRAY?

PAB CONVENIENCE TRAY is a medical device that received FDA 510(k) clearance on 1978-09-20. The listed applicant is Waters Assoc., Inc.. The 510(k) number is K781264.

When did PAB CONVENIENCE TRAY receive FDA 510(k) clearance?

PAB CONVENIENCE TRAY received FDA 510(k) clearance on 1978-09-20, under 510(k) number K781264.

Who is the listed applicant for PAB CONVENIENCE TRAY?

The FDA 510(k) record lists Waters Assoc., Inc. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for PAB CONVENIENCE TRAY?

The FDA product code for PAB CONVENIENCE TRAY is GAA.

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Other records listing Waters Assoc., Inc. 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.

K811975MODEL 480 VARIABLE WAVELENGTH ULTRA VIOLK8024817FRENCH FLOW DIRECTED TRIPLE LUMEN CATHK801852MRM-2 OXYGEN CONSUMPTION MONITORK801431PAN-AM MYELOGRAM TRAYK791661SYSTEM CONTROLLER 720 SERIESK7910264F STERILE BALLOON-LESS, CATHETER 913-28

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Related Devices (Code: GAA)

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.

K223625CapnoSpot™ Pneumothorax Decompression IndicatorPneumeric, Inc.K102274ARVIK LAPAROSCOPIC ASPIRATION INSTRUMENTArvik Enterprises/ Mini Lap TechnologiesK011586IRMA SL BLOOD ANALYSIS SYSTEM GL CARTRIDGEDiametrics Medical, Inc.K994151PERCUTX-INJECTION/ASPIRATION NEEDLE PROBES/DEVICESXimed/Prosure/InjectxK983200INJECTION/ASPIRATION NEEDLES PROBES/DEVICES-TPI/TPI FLEXXimed/Prosure/InjectxK974741MANAN ACCURA NEEDLEMedical Device Technologies, 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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