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FDA 510(k)

PIPETTE, DISPENSING, MODEL ADP-30SD

K-Number: K770772 · 1977-07-11

Decision Date1977-07-11
Product CodeJQW
Advisory CommitteeCH
DecisionSubstantially Equivalent

Device Summary

PIPETTE, DISPENSING, MODEL ADP-30SD is the device name listed in this FDA 510(k) record. The listed applicant is G.D. Searle and Co.. It received FDA 510(k) clearance on 1977-07-11 under 510(k) number K770772. The device is classified under product code JQW. It was reviewed by the CH advisory panel. FDA Decision: Substantially Equivalent.

Frequently Asked Questions

What is the PIPETTE, DISPENSING, MODEL ADP-30SD?

PIPETTE, DISPENSING, MODEL ADP-30SD is a medical device that received FDA 510(k) clearance on 1977-07-11. The listed applicant is G.D. Searle and Co.. The 510(k) number is K770772.

When did PIPETTE, DISPENSING, MODEL ADP-30SD receive FDA 510(k) clearance?

PIPETTE, DISPENSING, MODEL ADP-30SD received FDA 510(k) clearance on 1977-07-11, under 510(k) number K770772.

Who is the listed applicant for PIPETTE, DISPENSING, MODEL ADP-30SD?

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

What is the FDA product code for PIPETTE, DISPENSING, MODEL ADP-30SD?

The FDA product code for PIPETTE, DISPENSING, MODEL ADP-30SD is JQW.

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.

Other records listing G.D. Searle and 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.

View all 56 devices →

Related Devices (Code: JQW)

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.

Official Source

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Data sourced from FDA Open API. For the most current and authoritative information, always refer to the official record.

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