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FDA 510(k)

ALLERGIST PACK SYRINGES

K-Number: K771359 · 1977-08-22

ApplicantPharmaseal Div., Baxter Healthcare Corp.
Decision Date1977-08-22
Product CodeFMF
Advisory CommitteeHO
DecisionSubstantially Equivalent

Device Summary

ALLERGIST PACK SYRINGES is the device name listed in this FDA 510(k) record. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. It received FDA 510(k) clearance on 1977-08-22 under 510(k) number K771359. The device is classified under product code FMF. It was reviewed by the HO advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the ALLERGIST PACK SYRINGES?

ALLERGIST PACK SYRINGES is a medical device that received FDA 510(k) clearance on 1977-08-22. The listed applicant is Pharmaseal Div., Baxter Healthcare Corp.. The 510(k) number is K771359.

When did ALLERGIST PACK SYRINGES receive FDA 510(k) clearance?

ALLERGIST PACK SYRINGES received FDA 510(k) clearance on 1977-08-22, under 510(k) number K771359.

Who is the listed applicant for ALLERGIST PACK SYRINGES?

The FDA 510(k) record lists Pharmaseal Div., Baxter Healthcare Corp. as the applicant. This does not by itself establish the device manufacturer.

What is the FDA product code for ALLERGIST PACK SYRINGES?

The FDA product code for ALLERGIST PACK SYRINGES is FMF.

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Other records listing Pharmaseal Div., Baxter Healthcare Corp. as applicant

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Related Devices (Code: FMF)

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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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