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FDA 510(k)

AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190

K-Number: K882728 · 1988-10-06

ApplicantAmersham Corp.
Decision Date1988-10-06
Product CodeJJY
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190 is the device name listed in this FDA 510(k) record. The listed applicant is Amersham Corp.. It received FDA 510(k) clearance on 1988-10-06 under 510(k) number K882728. The device is classified under product code JJY. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190?

AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190 is a medical device that received FDA 510(k) clearance on 1988-10-06. The listed applicant is Amersham Corp.. The 510(k) number is K882728.

When did AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190 receive FDA 510(k) clearance?

AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190 received FDA 510(k) clearance on 1988-10-06, under 510(k) number K882728.

Who is the listed applicant for AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190?

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

What is the FDA product code for AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190?

The FDA product code for AMERLITE ENDOCRINOLOGY CONTROL SERA LAN.4190 is JJY.

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Other records listing Amersham Corp. 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.

K914135AMERLITE(TM) PROLACTIN-30 ASSAY, LAN.0086/2086K912733AMERLEX-M SPECIFIC ESTROL(UNCONJUGATED) RIA KITK912766AMERLITE CK-MB ASSAYK904666AMERLITE TSH-60 ASSAY PRODUCT CODE: LAN. 0008/2008K902760AMERSHAM TSH CONTROL SERAK901832GADOLINIUM-153 BONE DENSITOMETER SOURCES GDC.10415

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Related Devices (Code: JJY)

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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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