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FDA 510(k)

SYVA SAMPLE SEAL

K-Number: K844949 · 1985-02-15

ApplicantSyva Co.
Decision Date1985-02-15
Product CodeKIE
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

SYVA SAMPLE SEAL is the device name listed in this FDA 510(k) record. The listed applicant is Syva Co.. It received FDA 510(k) clearance on 1985-02-15 under 510(k) number K844949. The device is classified under product code KIE. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the SYVA SAMPLE SEAL?

SYVA SAMPLE SEAL is a medical device that received FDA 510(k) clearance on 1985-02-15. The listed applicant is Syva Co.. The 510(k) number is K844949.

When did SYVA SAMPLE SEAL receive FDA 510(k) clearance?

SYVA SAMPLE SEAL received FDA 510(k) clearance on 1985-02-15, under 510(k) number K844949.

Who is the listed applicant for SYVA SAMPLE SEAL?

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

What is the FDA product code for SYVA SAMPLE SEAL?

The FDA product code for SYVA SAMPLE SEAL is KIE.

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Other records listing Syva Co. 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.

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Related Devices (Code: KIE)

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.

K964588WATERS 515 HPLC PUMP (515)Waters CorporationK935666PERKIN-ELMER SERIES 200 LIQ CHROMATOGRAPHIC PUMPThe Perkin-Elmer Corp.K924347WATERS(TM) 996 PDAMillipore Corp.K914841CHROMATOGRAPHY CLINICAL USE 75JQRMillipore Corp.K911299EQUIPMENT/MATERIAL DECONTAMINATING KITRohm and Haas Co.K862506THE WATERS MODEL 990 PHOTODIODE ARRAY DETECTORMillipore Corp.

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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