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FDA 510(k)

EXTEMP-V

K-Number: K771759 · 1977-09-28

ApplicantPharmaco, Inc.
Decision Date1977-09-28
Product CodeGAA
Advisory CommitteeSU
DecisionSubstantially Equivalent

Device Summary

EXTEMP-V is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaco, Inc.. It received FDA 510(k) clearance on 1977-09-28 under 510(k) number K771759. 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 EXTEMP-V?

EXTEMP-V is a medical device that received FDA 510(k) clearance on 1977-09-28. The listed applicant is Pharmaco, Inc.. The 510(k) number is K771759.

When did EXTEMP-V receive FDA 510(k) clearance?

EXTEMP-V received FDA 510(k) clearance on 1977-09-28, under 510(k) number K771759.

Who is the listed applicant for EXTEMP-V?

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

What is the FDA product code for EXTEMP-V?

The FDA product code for EXTEMP-V is GAA.

Related Clinical Trials

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.

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Other records listing Pharmaco, 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.

K771760EXTEMP

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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